DE212013000027U1 - Devices for promoting female sexual well-being - Google Patents

Abstract

An apparatus for promoting sexual arousal in a female user, comprising: a tissue contacting chamber including a suction chamber; and at least two stimulators that at least partially hang flexibly within the suction chamber.

Description

FIELD OF THE INVENTION

Embodiments of the present invention generally relate to devices for promoting female sexual well-being and function. Certain embodiments are particularly useful for promoting, enabling, stimulating, or enhancing sexual desire, excitement, or satisfaction of a female person.

BACKGROUND OF THE INVENTION

Clitoral vascular thrush plays an important role in female sexual desire, excitement and satisfaction. Sexual arousal results in the relaxation of smooth muscle and arterial vasodilation within the clitoris. The resulting increase in blood flow causes swelling of the tip of the clitoris and increases sexual arousal. A variety of conditions can cause erectile insufficiency of the clitoris and reduced clitoral arterial blood flow. This can lead to the difficulty or impossibility of achieving a clitoral swelling. Female sexual well-being may also be adversely affected by a lack of subjective arousal, genital moisture, or organismic function.

The occurrence of symptoms ranging from lack of satisfaction to malfunction is high in women. For example, according to a National Health and Socialize study, in 1,749 women aged 18 to 59, 43% experience sexual dysfunction. Furthermore, sexual female dysfunction varies with aging, is progressive and prevalent among 30-50% of women, and 68-75% of women experience a lack of sexual satisfaction or "problems" (no malfunction in nature). In a national study of more than 31,000 women in the United States, 44.2% of women reported experiencing a sexual problem. According to other studies, over 53 million women (43% of the US population) have reported one or more sexual problems, and over 14 million women meet clinical criteria for female sexual dysfunction (FSD), with low desire being by far the most common problem ( reported by 46 million women) (cf. Spector I., Carey M. Onset and Spread of Sexual Dysfunction: A Critical Review of Empirical Literature. 19: 389-408, 1990 ; Rosen RC, Taylor JF, Leiblum SR, et al .: Dissemination of sexual dysfunction in women: results of a survey of 329 women in an outpatient gynecological clinic. J. Sex. Mar. Ther. 19: 171-188, 1993 ; Read S., King M., Watson J .: Sexual Dysfunctions in Primary Medical Care: Dissemination, Characteristics, and Evidence by the General Practitioner. J. Public Health Med. 19: 387-391, 1997 ; Laumann E., Paik A., Rosen R: Sexual dysfunctions in the USA, incidence and influence values. JAMA, 1, 281: 537-544 ; Schein M., Zyzanski SJ, Levine S, Medal JH, Dickman RL, Alemango SA: Frequency of sexual problems in general practitioner patients. Pham. Prakt. Res. J. 1988; 7: 122-134 ; Shifren JL, Monz BU, Russo TA, Segreti A., Johannes CB: Sexual Problems and Suffering in US Women: Dissemination and Correlations. Obstet Gynekol. 2008; 112 (5): 970-978; and Shifren, Obstet Gynekol. 2008; 112: 970-978 , Each of these publications is incorporated by reference.

Research indicates that adequate blood supply is required for good clitoral and vaginal functions and satisfying sexual experience at any age. Women at risk for female sexual dysfunction include those who use oral contraception, those with poor vascular health (those with diabetes, high cholesterol and high blood pressure), aging women and those who have undergone or have undergone cancer therapy (which may disadvantageously reduce moisture, hormone levels and / or genital sensation). The use of oral contraception may lower the blood levels of testosterone needed to regulate blood flow to the genitals and stimulate sexual desire, thus causing long term permanent sex hormone deficiency. Also, the prevalence of sexual problems increases dramatically with age, with 27.2% of women between the ages of 18 to 44 years, 44.6% of women ages 45 to 64, and 80.1% of women over the age of 65 years and older report sexual problems.

While the majority of male and female genitalia are similar, a subtle anatomical difference makes women more susceptible to inhibitors. While the glans in men and the clitoris in women alike each have the highest concentration of sensory receptors than any other location in the body, the male anatomy provides enhanced structural support for the glans. Action against male sexual dysfunction may benefit from this structural support by increasing or increasing venous fine function of the erectile tissue. In contrast, there is no anatomical supportive mechanism in women for the blood rush, which makes women more susceptible to a large number of strong inhibitors. While the female cavernous body is subjected to blood rush during the stimulation (s. ), he does not support the rush of blood to the same extent as the male anatomy.

illustrates a variety of factors that can act as inhibitors or promoters of sufficient sexual stimulation. Illustrated, for example such as sensory and psychosocial factors, such as the well-being of the woman's relationship with her partner, and emotional and visual cues and central nervous system (CMS) mediated promotion or inhibition of the drive (indicated by the +/- symbol). Other health factors such as diabetes or cardiovascular disease, or factors such as drugs, may promote other inhibition or promotion. This multifactorial network has made the development of a safe drug for the treatment of women very challenging.

The female sexual circle influences the occurrence of satisfactory sexual experiences (SSE) in women. The circle closes the stalls (i) emotional and physical satisfaction, leads to (ii) emotional intimacy, leads to (iii) being receptive to sexual stimuli, inducing (iv) sexual arousal, inducing (v) arousal and sexual desire which leads the circle back to the state of (i) emotional and physical satisfaction. Spontaneous sexual dynamics may occur between levels (ii) and (iii), between levels (iii) and (iv), and / or between levels (iv) and (v).

These and other challenges may be addressed by the embodiments of the present invention.

BRIEF SUMMARY OF THE INVENTION

Certain embodiments of the present invention relate to a system for promoting female sexual arousal; for clitoral blood flow by suction in combination with vibration stimulation; for providing a variable and adjustable control of vibration and suction; to provide a new force-tissue optimization scheme based on stimulators mounted on a flexible membrane; for providing a new embodiment of a Sauganbauteils in combination with multifocal actuators; and for providing new actuators for mechanical movement and suction.

Certain embodiments of the present invention relate to a system for providing a tissue-contacting chamber and at least two stimulators that are connected to the chamber and controlled so that the user experiences spatially-limited stimulation. The system may include a suction inlet in fluid communication with an interior of the tissue contacting chamber. The system may include a suction matching mechanism integrated with the tissue contacting chamber. The system may include a piston positioned within the interior of the tissue-contacting chamber and configured to adjust the suction within the tissue-contacting chamber. The system may include a sealing surface attached to the tissue-contacting chamber and configured to maintain a substantially air-tight seal against the tissue. The system may include a control unit and / or a remote control unit. The system may include controlling parameters of the stimulators, and that the parameters are selected from the group consisting of vibration frequency, vibration intensity, vibration duration, sequence of engine vibration, and combinations thereof. The system may include controlling the stimulators by selecting from a pre-programmed algorithm, a user-customizable algorithm, or combinations thereof. The system may include a suction device and a portable device body, wherein the suction generating device is detachable from the portable device body. The system may include maintaining the device body substantially in contact with the tissue after the aspiration-generating device is removed. The system may include a membrane that at least partially includes at least one of the stimulators. The system may include that the membrane is connected to the chamber. The system may include the membrane being configured to be displaced by the clitoris of the user. The system may include controlling the stimulators so that the user experiences a simulated macroscopic movement. The system may include stimulating the macroscopic stimuli upon tissue contact. The system may include that the vibration generated by one stimulator is isolated from the vibration of another stimulator. The system may include the vibration generated by a stimulator being isolated from a wall of the tissue contacting chamber. The system may include maintaining at least one of the stimulators in direct contact with the clitoris of the user during a suction application.

Certain embodiments of the present invention relate to a system for providing a mechanically stabilized housing, a suction chamber within the housing, and a plurality of stimulators. The system may include a flat housing. The system may include the housing being adapted to be portable. The system may include the stimulators configured to provide multi-dimensional stimulation. The system may include that the stimulators are configured to be a combination of macroscopic To provide movement and vibration stimulation. The system may include the stimulators configured to create a stroking motion.

Certain embodiments of the present invention relate to a system for providing a tissue-contacting chamber including a suction chamber, wherein the suction chamber is in fluid communication with a programmable suction pump, and wherein at least two stimulators are mounted within the suction chamber, the motors and the suction pump so are configured to be independently controllable via a control circuit. The system may include a control block that includes previously loaded vibration patterns and previously loaded suction patterns. The system may include the control block being configured to allow a user to create vibration patterns and suction patterns. The system may include a portable device body and a suction pump mounted in the device body. The system may include the control block being configured to allow a user to set a first suction level and a second suction level. The system may include that the control block is configured to allow the user to set a rate at which the suction pump alternates between the first suction level and the second suction level.

BRIEF DESCRIPTION OF THE DRAWINGS

to illustrate various views of a device according to an embodiment of the invention.

to illustrate various views of the internal component of a device according to one embodiment of the invention.

illustrates a membrane according to one embodiment of the invention.

FIG. 11 illustrates a perspective view of the body-contacting side of a device according to an embodiment of the invention. FIG.

11 illustrates in close-up a perspective view of the body-contacting side of a device according to an embodiment of the invention.

FIG. 11 illustrates a perspective view of the interior of a chamber part and an associated stimulator of a device according to an embodiment of the invention. FIG.

Figure 12 illustrates a perspective view of the exterior of a portion of the chamber and the associated stimulator of a device according to one embodiment of the invention.

FIG. 11 illustrates a perspective view of the interior of a chamber part and an associated stimulator of a device according to an embodiment of the invention. FIG.

FIG. 12 illustrates a perspective view of the exterior of a chamber member and associated stimulator of a device according to one embodiment of the invention. FIG.

illustrates stimulators and vibration isolators of a device according to one embodiment of the invention.

illustrates a wearable garment and apparatus according to one embodiment of the invention.

to illustrate various views of a device according to an embodiment of the invention.

to illustrate various views of a device according to an embodiment of the invention.

illustrates a portion of an apparatus configured to provide a macroscopic movement in accordance with an embodiment of the invention.

Figure 11 illustrates a portion of an apparatus configured to provide macroscopic movement in accordance with another embodiment of the invention.

illustrates an apparatus configured to provide a macroscopic movement in accordance with an embodiment of the invention.

illustrates a perspective view of a device according to another embodiment of the invention.

FIG. 11 illustrates a cross-sectional view of a device according to another embodiment of the invention. FIG.

and illustrate views of a device and an arrangement of such a device according to another embodiment of the invention.

and illustrate views of a device according to another embodiment of the invention.

illustrates a view of a device according to another embodiment of the invention.

illustrates a view of a device according to another embodiment of the invention.

and illustrate perspective views of a device and a removable suction element according to another embodiment of the invention.

FIG. 11 illustrates a cross-sectional view of a device according to another embodiment of the invention. FIG.

11 illustrates a cross-sectional view of an apparatus and a cross-sectional view of the control unit according to another embodiment of the invention.

and illustrate stimulator and lever arrangements according to embodiments of the invention.

and illustrate a device that provides macroscopic motion according to one embodiment of the invention.

to illustrate various views of a device according to an embodiment of the invention.

and illustrate a charging station and device according to an embodiment of the invention.

illustrates a charging station and apparatus according to another embodiment of the invention.

and illustrate views of a device and a control unit according to an embodiment of the invention.

and illustrate views of a device according to one embodiment of the invention.

illustrates a view of a device according to an embodiment of the invention.

Figure 11 illustrates a view of certain elements of the human female anatomy that are relevant to embodiments of the invention.

is a flowchart illustrating numerous inhibitors and facilitators of a satisfying sexual experience and their dependencies.

to illustrate the relationship between blood rush and vibration transmission.

to illustrate the use of various embodiments of the invention.

is a partial cross-sectional view of another embodiment of the invention.

to Figure 12 are side views of a portion of certain embodiments with various tissue contacting configurations.

and are plan views of a device with a removable flange connection.

is a perspective view of a removable flange connection.

and show a removable flange connection including a flange diaphragm.

is a side view of the removable flange connection.

and are respectively a side view and a perspective view of a cross section of the removable flange of ,

is a plan view of the flexible membrane of the suction chamber.

is a perspective view of an integrated device.

and illustrate a device body configured to sit comfortably and reliably on a user in multiple contexts.

Figure 11 is a perspective view of a device including an on-board manual pump.

to show various embodiments of the sealing flange connection.

to illustrate user interfaces for a smartphone-type control unit.

and illustrate a side view and a partial interior view of a device with motors in the device body.

illustrates a device with multiple motors that are free to vibrate and impact a tissue chamber.

to illustrate arrangements of stimulation elements for use in a device.

to illustrate a pen-like stimulation system and a supplementary stimulation device.

to illustrate a motor and system of gripping organs for stimulating tissue in a tissue or suction chamber.

to illustrate arrangements of gripping members in combination with at least one motor and at least one coupler for stimulating tissue.

and illustrate two views of a spatially-separated vibrating element driven by one or more motors.

to illustrate various embodiments of a device having stabilizing, adhering and / or securing features.

illustrates an embodiment of a device capable of concurrent intravaginal and clitoral seating and stimulation.

to illustrate embodiments of a clitoral engagement chamber and associated device body.

DETAILED DESCRIPTION OF THE INVENTION

The embodiments of the present invention described herein, including illustrations and examples, are useful for promoting female sexual well-being and function.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any materials that are the same or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred materials will now be described. All publications mentioned herein are hereby incorporated by reference to disclose and describe the materials in connection with the publications in which they are cited.

Brief summaries of particular terms are presented in the description of the invention. Each term is further explained and illustrated throughout the description, figures, and examples. Any interpretation of the terms in this specification should take full description, illustrations and examples as presented herein.

The singular terms "a" and "the", "the" and "the" include the plural forms, unless the context clearly dictates otherwise. Thus, for example, reference to an object may involve multiple objects as long as the context does not clearly dictate otherwise. Likewise, references to multiple objects may include a single object unless the context clearly dictates otherwise.

The terms "substantial," "material," and so on, refer to a significant amount or extent. When used in conjunction with an event or circumstance, the terms may refer to acts in which the event or circumstance exactly occurs or to occurrences where the event or circumstance is closely approximated by typical levels of tolerance or variability herein described embodiments to take into account.

The term "about" refers to a value, quantity or measure that is near or near the reference value. The amount of variation in the reference value, which is detected by the term "about", is one that is typical of the tolerance levels or measurement conditions.

The term "stimulator" refers to elements that provide stimulation by mechanical motion (such as vibration), electrical stimulation, temperature or other sensory stimulation.

Certain biological molecules and anatomical structures exist in a healthy woman to produce rush of erectile tissue from the vulva and clitoris. These molecules and structures allow stiffening of the underlying stratum on which the nerves in the clitoris are used. The effect of the stiffening is to allow for a more rigid projection and presentation of the clitoral structures for stimulation, and also to mechanically allow energy waves to be more efficiently propagated through the surface with less energy absorption by the tissue. As a result, a stiff clitoris mechanically stimulated by deflection, vibration and the like spreads these forces through a taut surface of the structure as losing energy within the loose connective tissue. Thus, means of producing a rush of blood (eg, by drugs or aspiration) may enhance sensation and cause other reflexive responses (eg, humidification and oxytocin release). Furthermore, the type and distribution of sensory nerve endings within the tissues of the clitoris and surrounding tissue explain why certain movements, pressures, vibrations and other stimuli provide better pleasure sensations than others. Vibration and suction are both capable of producing blood rush through the nitric oxide pathway, and thus both can increase the sensitivity to sexual stimulation. The two follow different neuronal / physiological paths. Double triggering with the help of vibration and suction in combination provides additive effects. Pacinia or pacini corpuscles, also called father-pacini receptors, conduct signals in response to vibratory "pressure" (tissue vibration is delivered via a pressure wave) - the reflex responses use NOS paths that extend into the same structures undergoing blood flow in the embodiments of the suction elements described herein. Movement / gliding in a repetitive pattern also creates a "pressure pattern" and vibratory nerve signals. Nerves can quickly adapt to the stimuli, so that vibration in a location typically becomes less influential, so moving the location of the vibration is beneficial, whether manual or automatic. All of the above is mediated by DH testosterone and other hormonal components (and therefore, testosterone therapy can help to improve the quality of the tissue as well as its "activity"), but we have discovered that through mechanical stimulation - either by suction or vibration or both - many of the hormonal pathways can be bypassed, and that reflex responses can be triggered directly.

We have discovered that combining blood gangrene with vibration together is a powerful combination, so that blood rush forms a more suitable mechanical backbone for the pacini-shaped body muscles that are to be stimulated, and that the application of both should simultaneously produce more profound effects than when used alone becomes. In both genders, the blood rush of the sexual organs is the key physiological goal in the sense that blood rush is crucial to achieving a satisfying sexual experience. As in the to is illustrated, vibration energy spreads better along a strained and perfused substrate. Embodiments described herein provide devices for the rush of blood of sexual organs to better disseminate vibrational energy.

Certain stimulation devices in the prior art, such. As vibrators, provide relatively diffuse stimuli. This means that the vibratory motion provided by a vibrator is applied relatively evenly across the clitoris and surrounding tissue. In certain vibratory devices capable of delivering vibration over a more narrowly focused surface, the frequency and magnitude of the vibration may still be a relatively diffuse vibratory motion on the clitoral tissue. In addition, much vibration of the prior art vibrators is lost in vibrating the handle, housing, and hand of the user or other parts of their body.

Advantageously, certain embodiments described herein are capable of providing complex suction patterns. Such complex suction waveforms may provide a comparatively organic stimulation experience as compared to mechanical stimulation devices in the prior art. For some users, the variable suction patterns and algorithmic waveforms of certain embodiments may induce thrush and stimulation such that effective arousal is achieved without the use of vibration.

Advantageously, and in contrast to prior art devices, the embodiments described herein are capable of providing spatially distinct vibratory motion. This means that a woman experiences spatially delimited vibratory motion. In certain embodiments, such spatially limited vibratory motion may simulate an experience of macroscopic motion on the clitoris. Macroscopic movement can be understood as an analog of stroking, tongue movement, or movement that coincides with sexual intercourse. For some users, the spatially limited vibrational motion of some embodiments may cause rush of blood and stimulation, such that effective arousal is achieved without the use of suction. For some users, the macroscopic movement on the clitoris, according to certain embodiments, can produce thrush and stimulation so that effective arousal is achieved without the use of suction.

One aspect of the spatially limited stimulation is the isolation of the stimulation generated by one stimulator from the stimulation produced by another adjacent stimulator. By isolating the stimulation generated by one motor from that of another, a device stimulates and / or mimics macroscopic movement on the clitoris. Another aspect of spatially limited stimulation is the isolation of the stimulation generated by a stimulator from the housing, which minimizes the loss of stimulation and allows the stimulation to be focused on the target tissue.

Another advantage of isolating vibration in devices according to embodiments disclosed herein is that a relatively small device can be worn discreetly that produces little noise while applying focused isolated vibration and subjecting the clitoral tissue to blood flow.

Certain embodiments of devices disclosed herein use suction to bring tissue into contact with vibratory elements. Certain devices remain in contact with tissue due to the suction applied to the tissue. However, another advantage of isolating the vibration in devices is that the airtight seal between the device and the tissue is substantially not separated by the vibration. This type of vibration isolation essentially involves isolating the closure elements of the device from the vibration elements in the device.

The compact size of the devices disclosed herein makes them inconspicuously portable, and enables them to be carried in a handbag. However, the devices disclosed herein are of such size and configured to be accessible and controllable during wear. Devices disclosed herein may be worn before and during intercourse, or as a program for attracting blood flow and nerve tissue sensitization. Devices disclosed herein may be adaptable and changeable and provide selectable variable suction and vibration characteristics. Devices disclosed herein may be capable of being remotely controlled, e.g. B. by means of a smartphone. Devices disclosed herein may be capable of promoting and / or maintaining female sexual arousal.

Advantageously, the devices disclosed herein use relatively low power motors to produce focused, spaced vibration.

According to certain embodiments, the device has some or all of the following features: (i) has a suitable seat; (ii) provides adequate stimulation; (iii) is sufficiently comfortable or bearable; and (iv) works reliably and safely.

With regard to suitable seating, the following attributes may be present in a device having a suitable seat: (i) the device is portable while walking without the need for a tether or additional garment; (ii) the device is sized so that the attachment surface fits between the labia majora below the clitoris and the housing leaves the labia majora above the clitoris; (iii) the device continually fits during the process of blood rush; and (iv) the device is portable during intercourse. Further, the device may be configured so that placing a portion of the device behind the labia major is sufficient to hold the device securely in place, with or without additional suction.

According to certain embodiments, a proper fit may be achieved by providing the following parameters: (i) the device design and center of gravity allow the device to hold on the tissue for at least five minutes without a tether; (ii) the device can be worn under clothing; (iii) the mass of the device allows retention only by suction; (iv) the device remains in place for at least five minutes without adaptation; (v) the device has a compatible tissue interface region; (vi) the device remains in place while the device is being worn standing or walking; (vii) the layout of the device attachment surface is anatomically appropriate; (viii) the device is designed to fit over at least one clitoral region of the woman; (ix) the device provides the tissue space to expand; (x) the external enclosure allows discrete use; (xi) the device is designed to neither obstruct the vaginal opening nor to restrict access; (xii) the device body can withstand a force which pushes it against a soft surface, such as a body; (xiii) Device height does not constrain partner interactions, and corner geometry is comfortable for both partners.

In certain embodiments, proper placement may be achieved by activating one or more motors to a perceived vibration level to allow the user to center the stimulatory effect on the clitoris. By pre-activating the motors during placement, the user can adjust the seat and determine the most effective location for vibration stimulation and / or suction stimulation.

With regard to appropriate stimulation, one or more of the following attributes may be present in a device to provide adequate stimulation To provide stimulation: (i) the device uses suction on the vulvar region or, more specifically, the clitoral region to allow for clumping of blood in the clitoral tissue; (ii) the device is capable of applying vibrational energy to at least the region of the clitoral tissue; and (iii) the device provides stimulation for a time sufficient to achieve the desired arousal.

According to certain embodiments, adequate stimulation may be achieved by providing some or all of the following parameters: (i) the device provides suction in the clitoral region ranging from about 0.7 "Hg to about 9" Hg; (ii) the device provides suction with the optional addition of an intimate lubricant in an environment where pubic hair occurs; (iii) the device maintains the selected suction level for a minimum of five minutes; (iv) the user can control the suction level and pattern, including by using a cordless remote control; (v) the device generates vibration within the frequency range of 100 to 300 Hz; (vi) the vibration forces (maximum to maximum) promote excitation under load; (vii) the vibratory elements are kept in direct contact with tissue when suction is applied; (viii) the device provides full power stimulation for a minimum of thirty minutes with a single battery charge; and (ix) the device is capable of moving the vibration between sources, as determined by the user.

In terms of comfort and portability, one or more of the following attributes may be present in a device that is sufficiently comfortable and bearable: (i) the device allows the user to release the suction, if desired; (ii) the device does not generate excessive noise; (iii) the device does not cause irritation to the urethra; and (iv) the device is comfortable to wear with tissue-contacting surfaces that are soft and pliable and / or smooth with no protrusions.

According to certain embodiments, sufficient comfort and portability can be achieved by providing some or all of the following parameters: (i) the user can release the suction within five seconds, if desired; (ii) the device does not generate noise exceeding 70 dB as measured at a distance of 2 "from the outside of the envelope when attached to the user; and (iii) the device fits over a woman's vulvar or clitoral region without obscuring the urethral opening.

For reliable and safe performance, the following attributes may be present in a device that operates safely and reliably: (i) the device presents no risk of electrical shock; and (ii) the device allows proper cleaning or disposal after each use.

In certain embodiments, reliable and safe performance may be achieved by providing some or all of the following parameters: (i) the battery and electronic spaces are isolated from unintended contact with liquids; (ii) the maximum discharge rate of the battery is not considered dangerous; (iii) device life can be rated at two to three years; (iv) the stimulators are rated for at least adequate use; (v) the device is water resistant when it is cleaned as recommended; and (vi) the device protects regions from contact with tissue / fluids or allows access to regions behind the tissue interface.

Certain embodiments have some or all of the following features: (i) the user is able to tailor the suction and vibration stimulation to their needs; (ii) the device resists stress of normal use; and (iii) the device can not have user-replaceable parts.

Specific aspects of the device features may include some or all of the following: (i) the user is able to adjust suction to a level that is comfortable; (ii) the user is able to remove the suction tube from the device without losing vacuum pressure that would lead to device detachment; (iii) the user is able to control the vibration function by means of cordless remote control; (iv) the user interface is via iOS Android or another mobile operating system application on a Bluetooth-enabled device or by means of an RF or Bluetooth fob-like controller key; (v) the user is able to control the vibration parameters such as pattern transition speed and vibration amplitude; (vi) power is provided by means of an internal rechargeable battery which is not accessible to the user; (vii) the user is able to control the vibration focus by pointing with his finger at a cordless device; (viii) the user is able to control a degree of engine overlap; (ix) engine overlap is optimized for a natural feel; (x) the device is capable of basic rotation engine patterns; (xi) the device resists external force applied to the outer shell (over the abutment surface) by the user; (xii) the envelope will withstand sufficient vacuum cycles without loss of integrity; (xiii) the user is able to customize the engine patterns including direction, engine selection, infinite loop, and save / recall of the custom patterns; and (xiv) the User is able to adjust the suction pattern and save / recall the customized pattern. Studies have shown that various areas of the female brain are activated when the clitoris itself is stimulated, as when the clitoris is stimulated by a partner, and that a woman can achieve orgasm more often by self-stimulation than by stimulation by a partner. With certain embodiments of the devices described herein, the woman may receive the stimulation patterns that allow her to achieve orgasm through self-stimulation and store it in the device memory. In the following, the device can be used during intercourse to play the stored patterns so that the woman can reach orgasm, so she would stimulate herself.

Preferred attributes of certain embodiments include: (i) user-adjustable suction for fixation and for blood flow dressing; (ii) user-adjustable vibration for blood flow attraction and for nerve stimulation; (iii) spatially delimited stimulation by macro-motion or isolation and control of multiple stimulation sources; (iv) harness-free portability during sexual intercourse; and (v) adaptability and reusability.

An embodiment of a device includes: (i) a shell that encloses a circuit and battery and connects to the suction zone; (ii) conforming wings to improve attachment; (iii) multiple stimulators attached to the inner wall of the compliant suction zone; (iv) motors insulated from the outer shell to minimize damping and non-specific vibration; and (v) suction applied by a removable applicator that causes walls to move inward to improve tissue contact.

In one embodiment of the device, a compartment is coupled with a squeeze ball to provide suction to the compartment. The squeeze ball may be integrated into the housing or it may be removable. The compartment is associated with adhesive wings that are capable of conforming to interact with tissue. The wings are designed to conform to anatomy, and may, for. B. include a butterfly-like shape. The wings can help stabilize the device and maintain contact with the device in the relevant anatomy. The edges of the wings and the tissue-contacting surfaces of the device are soft or rounded or both.

Certain embodiments of the apparatus include on-board circuitry, power, pumps, or other electronic features. For example, the device includes an antenna for interacting with a remote control, such as a remote control. As an RF antenna, a. The device includes a battery.

Certain embodiments of the device are controlled by a remote operator that is connected by a drive cable to the vibratory and / or suction elements within the portable part of the device.

Certain embodiments of the invention provide mechanical motion, preferably macroscopic motion, to simulate the naturally used movements by the female in stimulating the clitoris as opposed to the high frequency mechanical movements of certain prior art devices. Such embodiments provide multivariant stimulation of the clitoris by means of a stabilized platform. By mechanically stabilizing a platform, such. By suction, it is possible to produce a wide and large number of stimulatory effects directly against the clitoral target tissue. Such effects can be difficult to achieve with an unattached platform. Examples of macroscopic motions include rotational motion, linear stroking, low frequency thumb motion, and combinations thereof. Such macroscopic movements may be accompanied by vibration, e.g. As simple vibration or more varied and / or complex wavy vibration combined.

Certain embodiments of the device provide variable suction. In such embodiments, the user can quickly and easily adjust the level of suction. Further, in certain embodiments, variable suction is programmable such that the amount of suction applied by the device can be varied according to a pattern. In some cases, the suction pattern is tuned to the vibration and / or macroscopic motion patterns. The device controller includes means for controlling the suction patterns, the pre-loaded suction patterns, the user-adjustable suction patterns, or combinations thereof. The device controller allows the user to select pre-loaded combinations of a suction pattern, a vibration pattern, and / or a macroscopic motion pattern, and also enables the user to create and select customized combinations.

. . and illustrate different views of a device 100 according to one embodiment. device body 110 is designed to sit comfortably and discretely on the user's body while remaining accessible and controllable. device body 110 closes on-board control circuits, such as a circuit board, and also a user control pad. Alternatively or additionally, device body 110 an antenna for communication with a remote control device include. device body 110 may include a power source, such as a battery. device body 110 is with suction chamber 120 connected. suction chamber 120 closes sealing edge 125 which is capable of providing a substantially air-tight seal against tissue. sealing edge 125 can be a flange with a larger width than in the pictures to be. suction inlet 130 is in fluid communication with the interior of the suction chamber 120 and provides a connection to a suction device (not shown) that has a negative pressure within the suction chamber 120 generated. suction inlet 130 may also include a check valve or other one-way valve, so that when negative pressure to the suction chamber 120 is applied, the check valve or other one-way valve prevents suction loss through the valve. Optionally, device body 110 include an on-board pumping system to initial suction of the suction chamber 120 provide. Further, the on-board pumping system may include a pressure sensor to maintain the desired level of negative pressure in the pressure chamber 120 despite the presence of a leak along the sealing edge 125 can occur. Although not shown in this embodiment, device may 100 include the suction chamber, sealing members, stimulators or other stimulation features or combinations thereof as described in other embodiments herein.

. . . illustrate different views of the device 100 according to one embodiment. These pictures show vibration motors 180 inside the interior of the suction chamber 120 are arranged. In certain embodiments, the vibration motors 180 coin-type miniature motors having an eccentric rotating mass that provides vibratory motion. device 100 is designed so that the vibration motors 180 engage tissue when tissue enters the suction chamber 120 is sucked. The vibration motors 180 can get into the wall of the suction chamber 120 embedded, or they may otherwise be in connection with the suction chamber 120 to be appropriate. In certain embodiments, it is preferable to transfer vibration from vibration motor 182 on the housing of the suction chamber 120 to minimize. Preferably, the majority of the vibrational energy is applied to tissue contacting vibratory motors 180 transferred. The vibration motors 180 can with regard to vibration from the rest of the device 100 be isolated by using attachment mechanisms that facilitate the transfer of vibratory motion to the wall of the suction chamber 120 prevent. As described herein, the vibration motors 180 be addressed individually by the regulator circuit, so that movement patterns and in particular stimulations of macroscopic movement can be applied to the tissue that is in contact with the vibration motors.

and illustrate a charging station 2000 for a device 2200 and a fob-like key regulator 2300 , The charging station 2000 can by means of cable 2050 be plugged into a power outlet. device 2200 can in the equipment room 2250 be placed, and knobs 2300 can in the governor room 2350 to be placed. The walls of the room may have charging points such as charging contact point 2255 to charge the device battery. Or the battery of the device 2200 can be charged by induction. station 2000 may contain a battery of comparatively high capacity by means of the cable 2050 is charged, and which is capable of holding the charge, and also the battery with comparatively smaller capacity in the device 2200 recharge when station 2000 is unplugged from a power outlet. regulator 2300 can also be charged as described herein. shows device 200 in charging station 2 which has the same attributes as the charging station in and will be shown. That means the charging station 2 to charge the device 200 powered by induction, contact points or other means, and includes a rechargeable battery that is able to charge the battery in device 200 to load.

illustrates three vibration motors 180 in a membrane 190 are included. membrane 190 is configured to be inserted into the suction chamber of a device. membrane 190 provides a safe, comfortable and reliable protective barrier around the vibration motors 180 around inside the suction chamber. The protective barrier helps to reduce tissue irritation and provides a way to clean and reuse the device. As in shown, has membrane 190 a convex shape defining an inner part into which tissue is sucked. membrane 190 has at least one, but preferably more than one hole, perforations, slots or combinations thereof to allow membrane deformation and air flow. During use, when suction is applied through the suction inlet to the suction chamber, tissue enters the suction chamber against the membrane 190 sucked. membrane 190 deforms against the inner of the suction membrane, while making close contact between the vibration motors 180 and tissue is maintained. Figure 2 shows two of the vibration motors configured to be placed with the end against the tissue. Any number of motors may be used and any number may be configured to be placed vertically.

illustrates a perspective view of the tissue-contacting side of the device 100 according to one embodiment. In this embodiment, the vibration motors 180 spaced relatively close together, thereby forming a space as large as to approximate the volume of clitoral tissue to be engaged with the device. illustrates a close-up of the space for the clitoris tissue. suction inlet 132 is pictured at about the top of the clitoral tissue space. But the inlet may be attached laterally instead of at the top. Furthermore, suction inlet 132 be technically remote from the space for the clitoral tissue by a permeable membrane, a grid or other Absetzstruktur. In other words, a fabric or mesh screen may be via suction inlet 132 be placed to prevent tissue from being caught in the suction inlet. For example, an expanded PTFE membrane may be used as a settling structure to provide and maintain a vacuum path between tissue and suction inlet. Illustrates projections 133 forming a settling structure. Furthermore, suction inlet 132 are technically detached from the space for the clitoris tissue by a narrow channel that is too narrow for the clitoris tissue to penetrate. Furthermore, suction inlet 132 include many small diameter suction inlets located recessed between the protrusions. Such settling structures can be combined. Further, the motors may be sufficiently protruding or protruding from the surface of the flexible membrane (still being covered by the membrane) to function as settling structures that restrain tissue from blocking the suction inlet region. The demarcation structures work to prevent tissue suction inlet 132 completely covered, which could cause both a drop in vacuum flow as well as danger or pain to the tissue.

and show that the coin-type miniature vibration motors 180 deep in the membrane 190 reset so that one third to half of the engine is beyond the diaphragm 190 extends against the tissue. Deep resetting of the motors places them more on the tissue and provides a deeper space for the clitoral tissue. Close proximity to the tissue and deep space for the clitoral tissue can each provide higher stimulation forces compared to flat reset motors. It is advantageous to transfer as much power as possible from the motors to the tissue, especially in embodiments in which the device is held in contact with the tissue by suction. In such embodiments, it is advantageous to transmit the force effectively to the tissue because the motors are of relatively low power and because power losses will result in attenuating the stimulation effect.

and show channels 192 in the membrane 190 that at least partially the recessed parts of the vibration motors 180 surround. The channels 192 can be a thinned part of the membrane 190 and may be part of the membrane form or may be created by removing material from the membrane after it has been formed. channels 192 act to help provide and maintain a vacuum path between tissue and the suction inlet by providing a "leak path". As discussed above, it is advantageous in certain embodiments to have a flow path to the suction inlet 132 maintain. channels 192 also act to isolate the vibration of a given engine from the rest of the membrane and from the body of the device. By being thinner regions than the surrounding membrane, the channels can become 192 more bending and reducing or preventing loss of vibrational energy that would otherwise be transmitted to the relatively thicker and less flexible parts of the membrane. Minimizing or eliminating the transmission of vibration in the membrane to the device body has the advantages of avoiding undesirable effects such as noise, discomfort, reduced stimulation, and reduced suction (due to loss of the seal provided by the sealing edge).

and illustrate views of a suction chamber 120 and vibration motors 180 according to one embodiment. shows a view of the interior of the suction chamber 120 and shows stimulating features 185 that with the vibration motors 180 are coupled. When tissue enters the suction chamber 120 is sucked, transmit the stimulating features 185 Vibration energy generated by vibration motors 180 was generated on the tissue. stimulation features 185 can have a variety of shapes, textures and configurations. stimulation features 185 may be different in a single device and may be interchangeable, replaceable and customizable. shows a view of the outer surface of the suction chamber 120 and illustrates the arrangement of the vibration motors 180 ,

and illustrate the use of the suction chamber 120 and the miniature vibration motors 180 according to one embodiment. In this embodiment, the miniature vibration motors are 180 cylindrical in contrast to the disc-shaped coin-like miniature motors. vibration motors 180 are due to the stimulation features 185 coupled to transmit vibrational energy to the tissue.

illustrates a view of a device according to an embodiment. stimulators 180 are spatially spaced by isolation arms 188 , insulation arms 188 provide a sub-array in which the stimulators 180 can be arranged. Isolierarme 188 act by isolating the vibrational energy of one stimulator from that of another stimulator. This is useful in circumstances where the stimulators are activated at different times and / or at different frequencies and / or different amplitudes. By isolating the vibrational energy generated by one motor from the vibrational energy generated by another motor, it is possible to simulate macroscopic motion around or on the tissue. Figure 1 shows one type of vibration isolation, but other types and their equivalents are within the scope of this disclosure.

illustrates a view of the device 100 and an embodiment of a garment 50 , In this embodiment, the garment is 50 a simple strap or belt with the device 100 is connected and helps to keep it in its position on the user's body. In certain embodiments, the garment is 50 optional, as the device 100 is configured to maintain its position on the body primarily by suction. However, it is understood that for some users an additional means of maintaining the position of the device 100 may be desirable. Furthermore, it is understood that device 100 may be configured to be attached, or otherwise be integral with other garments including underwear or other feminine intimate apparel. Jewelry with functional elements that stimulates other areas of the skin can be used to increase arousal. Such functional elements may be one or more of air bubbles over the skin, stroking a soft element, application of gentle warming or cooling.

. . . . and show a device 200 according to one embodiment. device body 210 closes a suction chamber 220 one. suction chamber 220 closes seal and stabilization flange with a sealing edge 226 adapted to provide a substantially airtight seal against the tissue. suction inlet 230 provides fluid exchange between the inside of the suction inlet 220 and a suction device (not shown). device body 210 includes a user control panel, in this embodiment the trigger button 205 includes. It is understood that the user control panel may include various control inputs. Furthermore, device can 200 be controlled remotely. and illustrate a rear view of device 200 and show the inside of the suction chamber 220 , Multiple stimulators 220 are to the inner wall of the suction chamber 220 coupled. suction inlet 232 includes a check valve or other one-way valve that controls the suction inlet 232 with the interior of the suction chamber 220 combines. and show a sectional view of the device 200 and illustrate controller block in addition to the features already described 215 , regulator block 215 is electronically attached to the user control panel and / or remotely controllable by a remote control device by means of an antenna. device body 210 Provides a safe, reliable and comfortable protective barrier, protecting the electronics in the regulator block 215 protects.

Suction inlets may be connected to the suction devices using various types of fluid ports, including, but not limited to, snaps, quick disconnect sockets, screw jacks, luer lock sockets, drawer sockets, magnetic couplers and their equivalents.

device body 210 includes a strong but flexible shell that houses the electronics and electronics with the suction chamber 220 combines. device body 210 may further include a charging input to the power source in the controller block 215 is included, to charge. Trigger buttons present in the user control panel can be reset or otherwise made comfortable, safe and reliable.

sealing flange 225 may include soft, flexible, compliant material such as silicone, gel, or closed cell polyurethane foam, and optionally may be readily adhesive to the tissue, or may be adapted to contain an adhesive material. The foam or other material may also contain a lubricant which serves to close gaps in the seal between the sealing flange and the tissue. Other structures such as filament structures, e.g. As velor or corduroy or other woven or non-woven fabrics may be used in the sealing flange together with adhesives and / or lubricants to provide a secure fit, and to help minimize leakage paths. In some embodiments, a fabric used in the gasket flange may be moisture-responsive, such that it adheres or otherwise forms a firm bond with the skin and mucosa when the fabric becomes wet. The moisture may be from the user's body or may be in the form of a lubricant, adhesive or simply water or saline.

. . and illustrate different views of the equipment 200 according to another embodiment. device 200 closes a device body 210 a, a regulator circuit and a suction chamber 220 receives. The regulator circuitry can be accessed using a user interface located on the device body 210 is attached and / or by means of a remote control. The remote control can be physically attached to the device body 210 be connected or it can be connected cordlessly. suction body 220 closes seal and flange 225 adapted to provide a substantially airtight seal against the tissue. The different views of the . . and illustrate certain features of the shape and form of the device 200 , the comfortable, discreet and safe attachment of the device 200 promote. For example, device is 200 of a size such that the mounting surface defined by the surface is where the sealing flange 225 and suction chamber 220 meet, fits between the outer labia below the clitoris, and device body 210 leave the labia majora above the clitoris. Further, the taper of the upper section allows the suction chamber 220 comfortable, discreet and secure fit. The curvature of the body of the device 210 can help the device 200 adapted to the user, and allows discrete placement within the clothing.

In particular, the front section 225F of the sealing flange 225 is placed above the clitoris and stowed under the commissura anterior of the outer labium. In this position, the labia majora below the commissura anterior can become stuck with the beveled section 220t the suction chamber 220 engages, so that essentially the whole front and side parts of the sealing flange 225 stowed under the labia majora. Advantageously, the bevelled section allows 220t the suction chamber 220 in that the outer labia muscles engage comfortably with a comparatively narrow section of the device, while the vaginal tissue above the vaginal opening engages with the comparatively further sealing flange 225 engages.

Appropriate placement of the device 200 can be achieved easily and repeatedly through the following steps. If a user z. For example, when trying to place the device for the first time, you can use the use of a mirror so that the user's head and shoulders are supported, and she can use the mirror to watch herself while placing the device Open labia so that she can see her inner labia and the clad tip of the clitoris. Female users can identify a groove within their labia majora, which runs along the labia minora at the lower end to the wrapped clitoris at the top. device 200 can be effective when the sealing flange 225 is centered over the clitoris, and the relative ends of the sealing flange 225 to fit in the furrow. In some cases, the user may pull her outer labia to make room for the outer ring to seat it tightly in the furrow. The vibration motors can then sit tightly around the tip of the clitoris. In some cases, the user may apply a variety of lubricants (eg, water based lubricant) to her inner and outer labia, the tip of the clitoris, clitoral wrapping, and the comparatively soft edges of the sealing flange 225 to brush. By using the sensation of the low power vibrations as a guideline, the user can ensure that the clitoris is firmly seated within the space defined by the internal parts of the vibration motors. In some cases, the user may apply stimulation with her labia minora separate. A properly placed device sits high enough on the user's vulva to effectively deepen the clitoris rather than blocking the urethra or vaginal opening.

In certain embodiments, a plurality of vibrating discs or coin-type miniature motors are embedded in the wall of a flexible suction chamber. In certain embodiments, the motors are embedded in a flexible membrane attached to the walls of the suction chamber. When a suction is applied, the tissue is brought into contact with the stimulator. The motors may be controlled by a regulator circuit to produce one or more of the following patterns: (i) all on; (ii) clockwise; (iii) counterclockwise; (iv) up / down; (v) transverse; (vi) all pulsating; (vii) selected motor pulsing; (viii) gradients in frequency; and (ix) gradients in amplitude. The propagation of the vibration patterns and the spatial isolation of the motors can produce a desired effect of simulating macroscopic motion without the inclusion of parts that actually move in macroscopic dimensions. The flexible component reduces or eliminates the connection from engine vibration to the instrument housing and increases or maximizes energy delivery into the tissue.

In an in illustrated embodiment, the patterns are created by three vibration motors. For example, the rotation patterns (clockwise or counterclockwise) are generated by first applying motor 180a is activated, and then engine 180b is activated, and then engine 180c is activated. After a motor is activated, it can be completely deactivated, or its power can be reduced so that a Pattern of higher vibration force around the arrangement of the motors rotates. As another example, a V-shaped vibration pattern is created by simultaneously activating the motors 180a and 180b , whereupon both are deactivated, and then at the same time the motors 180a and 180c are activated, which are then both deactivated. The V-shaped pattern can then be repeated. As another example, a transverse pattern is created by alternately activating and deactivating the motors 180b and 180c , being engine 180a remains deactivated. As another example, a transverse pattern is created by alternately activating and deactivating the motors 180b and 180c , being engine 180a remains activated.

The patterns and equivalent patterns described above may be produced by an arrangement with more than three motors. Rotating patterns, transverse patterns, vertical patterns and combinations thereof can be created by selectively activating and deactivating the motors. All such patterns are within the scope of the invention disclosed herein, regardless of the number of motors. Further, in embodiments that depict engines that provide stimulation, other stimulators may be used instead of or in addition to the vibration motors. That is, one or more of the vibration motors may instead be an electrical stimulator, temperature stimulator, or other stimulator.

In certain embodiments, multiple vibratory motors produce resonance or diphasic amplification. Resonance or diphasic amplification patterns may be advantageous because they can create unique vibrational patterns that would be difficult to achieve with a source of vibration, and they can produce amplification of the vibratory force that exceeds the potential of a single motor. Such amplification may be useful in the case of certain electrical current or space limitations. Resonance or diphasic amplification generated by the use of multiple sources of vibration can employ a variety of sources, including rotary, linear, and piezoelectric. The combination of multiple sources can produce a wider range of customizable and selectable resonance patterns. Furthermore, motors of different size and / or strength may be used to generate multiple resonant frequencies to amplify the vibratory effect.

Multiple isolated and independent motors can be combined to produce diphasic amplification or resonance patterns and / or can simulate macroscopic motion. Transitions between the motors are softer with sine waves than with square waves. Optimizing the timing and amplitude of movement during the transition enhance the natural feeling of stimulation. Preferably, multiple small motors are used to provide easily differentiable stimulation and simulation of macroscopic motion. Small eccentric motors placed on edges provide a focused vibration point, which promotes differentiation between different sources of vibration. Slower vibration transitions promote differentiation between different sources of vibration compared to faster transitions.

In certain embodiments, devices provide macroscopic motion in addition to or instead of simulating macroscopic motion.

shows a device 300 , which provides macroscopic motion according to one embodiment. device 300 closes a suction chamber 320 and a sealing edge 325 which are both configured to engage tissue as described herein. In this embodiment, the suction chamber 320 flexible and deformable, allowing engine 380 the suction chamber 320 deformed while holding the suction chamber 320 by means of rails 370 crosses. engine 380 can be connected to a cylinder, or can itself be a cylinder running along the rails 370 rolls, slides or otherwise moves. The movement of the engine 380 through the suction chamber 320 simulates a stimulating petting movement and promotes blood flow and / or clitoral blood rush. suction chamber 320 includes a suction inlet (not shown), which is used the same as suction inlets described herein, and includes a check valve or other one-way valve to maintain suction in the chamber. engine 380 In addition to traversing on the rails 370 vibrate and thereby provide both a stroking motion and a vibratory motion.

shows an embodiment of device 400 , which provides macroscopic motion according to one embodiment. device 400 closes a device body 410 and a hood 420 one. Hood 420 is configured with respect to the device body 410 to rotate an axis that centers both to the device body 410 as well as the hood 420 is. stimulation features 485 are with the hood 420 connected. suction inlet 430 works to suck into the interior of the device body 410 to generate tissue in contact with the stimulation features 485 in a humorous. A motor (not shown) drives the rotation of the hood 420 in relation to the device body 410 and rotates stimulation features 485 on the clitoral tissue, which is in the interior of the device body 410 was sucked. stimulation features 485 can also be powered by vibration motors that provide both stroking and vibratory motion.

Alternatively, the movement of the hood can be magnetically driven. For example, hood can 420 include a single offset magnet. device body 410 may include a plurality of electromagnets, which are individually controlled by a controller. The movement of the hood can be driven by selectively charging each electromagnet in a sequence or pattern.

shows an embodiment of the device 700 in which a moving profile 775 under a stationary membrane 790 macroscopic movements for stimulation. The moving profile 775 is under a thin membrane 790 which is adaptable and flexible, and moves with the features on the profile. The profile 790 has elevated regions 777 that are spaced apart at physiologically relevant distances. The profile runs on two or more roles 779 of which at least one is driven to make the profile turn.

illustrates a device 500 according to one embodiment. device body 510 is on a flange 525 configured to maintain a substantially airtight seal against the tissue. The tissue-contacting surface of flange 525 may include a mild adhesive, and / or an adhesive substance may be present on the tissue-contacting surface of the flange 525 be applied. Optionally, a lubricant and / or an exothermic substance on the tissue-contacting surface of flange 525 be applied. flange 525 is flexible and compliant and adapted to provide a reliable and secure anatomical fit. device body 510 includes a suction chamber (not shown) capable of pulling tissue into its interior. device body 510 closes vibration motors 580 which are capable of delivering spatially separated vibrations to a tissue. device body 510 closes a trigger button 505 at a user-accessible location, for example at the side of the exterior of the suction chamber.

illustrates a device 600 according to one embodiment. device 600 closes a suction chamber 620 configured to apply suction to a tissue through a suction inlet or other mechanism described herein. device 600 closes a stimulator 680 and a power source, such as a battery. stimulator 680 is by means of an adjustment arm 640 in the suction chamber 620 set. Anpassungsarm 640 allows a user to control the force of contact between stimulator 680 and to control tissue precisely and repeatably. device 600 closes an activation button 605 and may include remote control capabilities via an on-board antenna. Alternatively, the adjustment arm may be electronically controlled, such as by applying a current through a nitiolar to control the position of the motor with respect to the tissue.

and illustrate an embodiment of apparatus 800 which is a thin flexible membrane 810 which is adapted to transmit a pulsating wave along its length. A flexible electronic controller 850 drives one or more flexible actuators 860 at least partially in the thin flexible membrane 810 are included. The flexible membrane may have a curved configuration defining an interior chamber. Sucking may be applied to the inner chamber by various mechanisms, including a deformable suction chamber 820 attached to the membrane 810 is appropriate. When the membrane is exposed to air, a mild exothermic reaction optionally occurs, which stimulates further blood flow.

In one embodiment of the device, the device could generate a sweeping wave motion. The speed and amplitude of the wave is variable, selectable and customizable in real time. The wave motion can also be used to deliver therapeutic substances directly to the genital region. The substances can be stored in the polymeric adhesive region or immediately behind the adhesive region. The mechanical displacement algorithm, or alternatively an algorithm focused on delivery, could be used to deliver the drug at the desired rate. Thin film actuators include shape memory polymers and metals, ferroelectric thin films, polymeric thin films, piezoelectric films, polymer / metal composites, and combinations thereof. Light or electromagnetic radiation can be used to drive the actuators.

In certain embodiments of the invention, wave motion can be achieved by sequentially loading regions of the thin film actuator. By stressing a given region, this region undergoes a conformational change that causes a local shift of the structure. Different tempo space patterns can be created to simulate a stroking motion. Alternatively, some regions may be made to vibrate, while all other regions offer simulated stroking. The thin film may be an electrically activatable polymer, a piezoelectric material A shape memory polymer, a shape memory metal or a composite material containing one or more of the following materials: metals, polymers, particles, stripes, charge elements, water, salt, bases, acids, etc. In some embodiments, the thin film actuator is formed from graphene, which is capable Being powered by current to provide vibratory stimulation, simulated macroscopic motion and / or macroscopic motion.

and illustrate an embodiment including a magnetically-bonded thin-film actuator 900 and regulator 950 , The thin-film actuator 900 is applied to the clitoris serving, and the regulator 950 is placed in the vaginal cavity. The regulator 950 provides a variable electromagnetic energy wave to the thin film actuator 900 , which makes the actuator vibrate. When the electromagnetic energy is provided by means of a rotating magnet, the magnet may be eccentrically supported by weight. Such eccentricity allows for local vibration or may also be weighted such that only the thin film actuator is vibrated. The thin film may be disposable and include other magnetically attachable material. The controller may be on board or removed from the device. The density of the magnetic element allows a variable focus of the drive along the surface. It can be an adhesive layer 910 such as a mildly adhesive polymer layer to adhere to tissue. The vibration is caused by electromagnetic activation of the magnetic layer 915 which is located between the adhesive layer 910 and the surface layer 920 located. The controller includes a rotating magnet, a motor, circuits, and the power source, such as a battery. The regulator can be included for safety, reliability and comfort.

In another embodiment, a regulator may be placed in the interior of the vagina and physically tied to a device placed over the clitoris. The controller and the device can be connected by means of a deformable connecting part, in order to allow a comfortable and compatible positioning of the device. Advantageously, by moving the relatively heavy controllers and power components from the clitoral device to the vaginal device, the clitoral device may become more comfortable and portable. The vaginal device may also include stimulation features, such as vibration motors.

illustrates an embodiment of apparatus 1100 in which a stimulator 1180 in contact with the top or front surface of a suction chamber 1120 stands. device 1100 closes a flange 1125 which provides a substantially air tight seal with the fabric while being reasonable, comfortable and portable. suction chamber 1120 Sucks tissue into its interior using a separate suction device or by deforming the suction chamber before the device 1110 was brought into contact with the tissue. When tissue enters the suction chamber 1120 sucked, stimulator can 1180 (or more than one stimulator) can be used to stimulate clitoral tissue. stimulator 1180 (or motors) can through a user control panel on device 1100 controlled or remote controlled.

Certain embodiments of the invention take advantage of a wide range of contributions that are wider than the contributions available from certain prior art devices. For example, the input may include complex waveforms, such as literally music or overlaying waveforms that make up the type of a song. The multiple oscillations of a "song" can produce a desired mechanical effect on the tissue-contacting actuators. The location or spatial arrangement of these "songs" could be differentially distributed across the target tissue surfaces to produce enhanced effects. For example, some regions may be more optimally stimulated by low frequency patterns, in other areas by high frequency patterns. High amplitude patterns in combination with variable medium to high variations are also possible. By spatially adjusting these effects, the simulation of manual stimulation, stimulation with the tongue, or sexual intercourse can be achieved. Multiple stimulus signatures are available to the user to create various effects. Nominally, some tissues may respond more to a simulated "rubbing effect" and more to cyclic "push" or thumb effects. The "songs" can be downloaded on a separate player or on the device itself using web-based media marketplaces, such. B. iTunes. illustrates a device 1200 , which is an arrangement of acoustic-mechanical drives 1282 or voice coils (eg, "speakers") to produce a variable selection of stimuli across the surface. Every drive 1282 is individually controllable by a controller to produce complex waveforms and pacing patterns as described herein.

and illustrate the interaction of a device 1300 and a separate suction device 1320 , The combination of device 1300 and suction device 1320 provides a kit for use according to the embodiments described herein. device 1300 includes a suction inlet in fluid communication with the interior of a suction chamber (not marked) on the device 1300 stands. suction device 1320 is as a suction device from tip type, but other suction devices are within the scope of this disclosure. A separate suction device allows a precise, repeatable and reliable suction application as well as discrete and comfortable carrying of the device 1300 ,

illustrates an embodiment of apparatus 1400 in which a stimulation feature 1485 is driven by a motor, which is in a device body 1410 is included. device 1400 is contacted with clitoral tissue by suction means described herein or by placing the device in close contact with tissue by means of a garment or garment-like device. stimulation feature 1485 provides macroscopic movement to stimulate clitoral thrust by providing a more natural paw and / or tongue movement as compared to vibratory motion. device 1400 may include one or more stimulation features.

In certain embodiments, the controller is designed to record user movements on a control surface to the tissue-contacting surface of the stimulating part of the device. By pressing their fingers onto the control surface, the user can create various levels of pressure to achieve vibration at the corresponding location on the tissue-contacting surface. By moving her fingers across the control surface in the optimum manner desired, a sequence of movements, pressures, vibrations and / or stimuli is created which mimic these movements on the tissue-contacting surface. These movements and inputs may be stored either locally on the device or at a level of control and replayed when it is desired to produce the desired effect without requiring the user to repeat their input patterns.

illustrates an embodiment of apparatus 1500 using a touchpad device 1550 can be remotely controlled to provide precise and customizable stimulation. Touchpad device 1550 can be a smartphone or an equivalent device. device 1500 closes an electroactive layer 1580 which directly touches tissue or contacts tissue through a thin membrane. Tissue gets in contact with the electroactive layer 1580 sucked as described herein. device 1500 closes a power source 1515 , a local regulator 1505 and an antenna 1535 one. The electroactive layer 1580 is configured to control the movement and pressure by the user's fingers on the touchpad device 1550 was applied to the clitoris tissue within device 1500 to imitate.

In certain embodiments, a remote controller is a controller configured to transmit radio frequency signals to the user-worn device. The controller may be of a size similar to a key fob remote control commonly associated with automobiles. A key fob-like remote may include various buttons and be capable of controlling the full range of the functions of the device discussed herein. and illustrate a key fob-like remote 206 and device 200 which has a coordinated housing space 202 includes, so the remote control 206 docked with the device and can be picked up there when not in use or even when in use. In general, the regulator circuit may include a circuit board, amplifiers, and radio antennas (including Bluetooth antennas).

Devices using low power Bluetooth or other radio antennas may experience broken connections when the remote control / device pair is disconnected by removal and / or physical obstruction (such as the user's or partner's body). In such cases, it is desirable to remain operational with respect to the device under the operating conditions prior to the tearing of the connection by the remote control automatically attempting to reconnect to the device. In other words, it is undesirable for the user or the partner to manually restore the Bluetooth connection between the remote control and the device if the mutual connection is lost during use of the device. And it is undesirable in terms of the device that the operation stops under the existing conditions before signal disconnection when the mutual connection is lost. Therefore, certain remote controls are configured to automatically reconnect to the device without the intervention of the user.

In situations where the remote will automatically reconnect to the device, it is important for the remote to poll the device for current device operating conditions. That is, it is desirable that while the device has maintained a status of operating conditions during the connection loss, the remote control does not interrupt the device operating conditions when the interconnection is restored. As a counter-example, in some Bluetooth pairings, after the pairing connection is established, the "master controller" will send a reset signal to the "slave device". Such a reset would be undesirable in circumstances where that Device with set parameters, patterns or programs in operation, because these parameters, patterns or programs would be interrupted by the reset signal. Such an interruption could be detrimental to the user experience.

In certain embodiments, the controller is physically attached to the device worn by the user. The tether may include electrical connection and also a fluid connection to provide suction to the suction chamber of the device.

In certain embodiments, the stiffness of parts of the device, such as the suction chamber, an arm holding a vibration motor, or a pacing feature may be controlled by moving a stiffening member such as a stylet inside or outside a receiving volume in the part whose stiffness is being controlled.

illustrates an embodiment of a device in which stimulator 180 with the end of lever 185 connected is. lever 185 has an internal receiving volume for receiving a stiffening stylet. By stiffening lever 195 attached to the body of the device or to the suction chamber, such as in shown chamber, can be attached, stimulator 180 to be tighter engaged with tissue. shows an embodiment in which lever 195 with oscillation motor 180 connected to the suction chamber 120 is appropriate. lever 195 is thus driven, a larger movement at its outer end in relation to the smaller movement of the oscillation motor 180 exhibit. In such an embodiment, leverages 195 the perception of macroscopic motion using relatively small motions of the coupling motor.

and show an embodiment in which a stimulator 180 within the suction chamber 120 is appropriate. shows a sectional view in plan view and illustrates a mechanism including two levers 195 and two pivot points 196 , The pivot points and levers cooperate to stimulator 180 to paint over the target tissue. While the mechanism is depicted with two levers and two pivots, other combinations of mechanical elements are possible, provided that they produce a controllable, stroking or stroking motion over the target tissue. shows a final section drawing, the stimulator 180 both as stroking over the tissue and around the longitudinal axis of the lever 195 turning illustrated. In certain embodiments, the rotating motion is passive and conforms to the shape of the tissue to provide substantial contact between the stimulator 180 and to maintain target tissue. In other embodiments, the rotational movement is actively controlled and may be used to deliver a more stimulating force to the target tissue. For example, as described herein, miniature coin type motors having an eccentric mass provide force when placed on the tissue at the edge. By actively turning the motors, differential force effects can be achieved. pivot point 196 may be both passive and active in the sense that there may be motors capable of propelling a stroking motion, or they may be comparatively simple joints that allow the motor to be moved across the tissue by means of a driving force at one of these points within the housing of the device.

One of the embodiments of the device provides suction to force and stiffen the blood in the tissue and vibration to stimulate the region. In other embodiments, the device provides suction for urging the blood into the tissue and stiffening it, as well as electrical or neutral stimulation for stimulating the region. In other embodiments, heating or cooling is employed, including light or infrared energy (eg, near infrared light emitting diodes) instead of vibration or electrical or neutral stimulation, or combinations of these stimulation types. The stimulation source is preferably in intimate contact with the tissue to optimize energy transfer.

Attachment of the vibration sources may also allow isolation so that there is a spatial separation between the sources and minimal diffusion of vibrational energy to adjacent structures in the device or tissue. Attaching the stimulators to a flexible membrane that travels with the tissue as it undergoes a rush of blood under suction can accomplish these goals. However, the membrane should have a direct path between the suction source and the tissue - if there is no path, the delivered suction will be significantly less. Placing holes or slots in the membrane can allow sufficient vacuum and energy transfer. However, holes and slits placed in the membrane may allow fluid from the tissue to pass through the membrane into the interior of the vibration region of the device.

and illustrate a plan view and a cross-sectional view of an apparatus according to certain embodiments. device 200 closes a device body 210 and a suction chamber 220 one. suction chamber 220 closes sealing flange 225 including a sealing edge 226 one which is so adapted, one essentially provide airtight seal against the tissue. suction inlet 230 provides fluid exchange between the inside of the suction inlet 220 and a suction device (not shown) that may be removable or may remain attached. device body 210 closes a user control panel 215 one. It is understood that the user control panel may include multiple control inputs. After that, the device can 200 be controlled remotely. Several vibration motors 280 are with the inner walls of the suction chamber 220 connected. suction inlet 232 closes a duckbill valve 238 (or a check valve or other one-way valve), the suction inlet 232 with the interior of the suction chamber 220 combines. device body 210 includes a strong but flexible shell that houses the electronics and connects the electronics to this suction chamber. device body 210 may further include a charging input for charging the power source in the regulator block 215 lock in. Trigger buttons present on the user control panel may be reset or otherwise made comfortable, safe and reliable. sealing flange 225 may include soft, flexible, compliant material (eg, silicone) and may optionally be slightly adhesive to the tissue or may be adapted to contain adhesive material. device body 210 is configured to be the back or bottom of device body 210 in another plane lies as a sealing flange 225 , This configuration allows device body 210 to stand over the user's pubis and optionally be attached to a garment while the gasket flange 225 is in contact with tissue.

shows intake manifold 231 , the suction inlet 232 with the suction inlet 230 combines. The suction tube material is selected to be resistant to adhesion of biological material. The path of the draft tube through the instrument housing can be configured to account for pressure drops and to avoid areas where liquid could accumulate. The suction tube provides an additional barrier between liquid and the electromechanical and electrical components within the inner housing of the device body.

In embodiments that include a suction tube, there is a pressure differential between the chamber above and below the membrane. When suction is applied, the area above the membrane is under higher pressure than the area below the membrane, causing the membrane to move down toward the tissue, thereby increasing the contact forces between the motors and the tissue. This pressure difference mechanism can be actively used to increase energy transfer.

The challenge of cleaning fluid from the interior regions of the device is addressed by enabling the flexible parts of the suction hollow body to be removable from the housing so that it can be cleaned by the user. Alternatively, as in and As shown, a tube may establish communication between the suction tube and a single hole in the membrane. The interior of this hole may have features (eg, protrusions, permanent shielding, etc.) to avoid tissue clogging the hole when vacuum is applied. In this case, liquid would no longer be able to enter the interior surface of the device and would be confined between the tissue surface and the suction tube channel. These regions could be flushed by the user without disassembly.

To tackle the challenge of cleaning, it is in another embodiment, as in , no fluid allows the interior 282 from device 200 enter, leaving the surface under suction chamber 220 and all of the external surface of device 220 easy to clean with soap and water. The inner 282 may be vacuum-sealed or contain a gel or liquid. The embodiment of device 200 in has a non-deformable button 284 , stud 284 has an O-shaped ring 286 making a seal around the button. stud 284 is on a pen 288 attached, so if button 284 Depressed and released, he returns to his starting position. sealing flange 225 creates a seal primarily at the sealing edge 226 with the fabric of the woman. suction chamber 220 is a compliant membrane tube that is biased to return to its starting position. Moving button 284 Forces a downward pressure on the yielding diaphragm hood, removing air from the suction chamber 220 herauszwingt. The sealing flange 225 In contact with the tissue acts as a one-way valve, and when the button is released, the yielding membrane tries to return to its original position, thus creating a suction under the sowing chamber 220 to create a negative pressure over the clitoris and promote blood rush. A biasing member may be added to the suction chamber hood to increase recoil.

shows a view of device 200 with the outer housing removed. regulator block 215 (or the board) is below the outer housing and between the suction inlet 230 and the trigger button 205 added. activation button 205 Of course, it is ready for operation with the controller block 215 connected, as well as I / O input 218 , In I / O input 218 A connection cable (or a connection input in a holder) can be plugged in which can be used to program and / or load the device. battery 212 is below the controller block 215 ,

Certain materials may be preferred for use as an actuator in devices described herein. For example, electroactive polymers expand and contract upon application of electrical current and may include taxa (focus points) to increase resolution. Electroactive polymers can be packaged in dense arrays that are highly customizable and have a good frequency range. Some designs have an extremely flat profile. Piezoelectric materials are another example. Piezoelectric crystals produce step function motion that can be used for rotary or linear motion and / or vibration. Piezoelectric materials can be miniaturized and incorporated into electronics and show a good frequency range. Another example is voice coils in which linear motion is created by creating an electric field around a magnet. Voice coils can achieve high amplitude, low voltage, and are smaller than coin counting miniature motors.

Voice coils can also provide more control flexibility than rotary motors - the frequency and amplitude can be decoupled from each other. Voice coils also allow greater isolation of the vibrational energy because only the moving elements vibrate and the housing is essentially stationary. This can allow greater spatial delimitation.

Certain actuator materials may be used to form an actuator assembly that provides high spatial resolution for vibration. For example, an arrangement that provides fourteen sources of vibration can improve the sense of motion that is delivered to the user and can provide significant customizable modes. In this example, each vibrating node is 4 mm in diameter, which is significantly smaller than the 8 to 15 mm diameter coin counting motors. A vibrating node of 4 to 6 mm in diameter would be desirable for this application to achieve the desired resolution.

Certain embodiments are capable of undergoing kinesthetic forces (or macroscopic motions such as palpation and rubbing) using an array of vibration motors. Devices disclosed herein are capable of (or at least simulate) kinaesthetic (or macroscopic) sensations using actuators that typically only provide tactile sensations. Devices capable of producing a convincing, natural-feeling palpation sensation rely on the coordination of: (i) motor spacing in the assembly (preferably, the motors are spaced about 1 to 4 mm apart); (ii) field width of each motor; (iii) traversal rate of a pattern played on the engine; and (iv) overlap.

According to certain embodiments, the devices manufactured and described herein are capable of tuning strength, traversal rate and overlap to the fixed physical parameters such as motor spacing, skin contact, etc. Various algorithms allow independent control of engine power, traverse rate and overlap. In an apparatus fabricated according to the embodiment and disclosed herein, an algorithm has been implemented in a low cost embedded microcontroller. Three input parameters were varied by remote control using low-power Bluetooth components that communicate from an iOS device (iPod iPhone 5 generation) to an embedded micro-controller (Texas Instruments CC 2540) to ultimately set these algorithm input parameters. The algorithm output controlled the pulse width modulated drives for all three to five motors simultaneously. The algorithm also allowed unique patterns so that the user could specify the order of traversal through the motor assembly. Different profiles, eg. Rectangle, sine curve, inclined plane, were used to make different motors at different rates as the patterns progressed through the motor assembly.

For motors with a non-linear response curve, pilot techniques (or feedback control if sensors are built into the device) can replace such response curves. Therefore, the motors start off with a time lag, unless instructed otherwise, so that the coordination discussed above can be achieved. In some embodiments, an accelerometer may compensate for gravitational effects.

Coin-type miniature vibration motors having an eccentric mass are used in certain embodiments. Generally, coin-type motors require larger masses and higher force to increase the stimulation power delivered to the device. Therefore, the stimulation force in eccentric motors is a function of mass, and more force is needed to drive that mass. In certain embodiments described herein, despite the relatively high mass and relatively high power of the motors, the devices may deliver spatially-isolated vibration through the isolation structures as described herein. Even if the motors are positioned relatively close to each other, to a seat with the clitoris provide the embodiments described herein substantially vibration isolation, and provide the user with a spatially delimited stimulation experience.

In certain embodiments, modified voice coils are used as stimulators. As described above, voice coils can achieve high amplitude, low voltage, and are smaller than miniature coin type motors. Voice coils may be modified to include a mass attached to the membrane driven by the electric field. Advantageously, such weight-bearing voice coils maintain the desired characteristics of the voice coil, including fast response time, independent control of frequency and amplitude, high acceleration, high-precision force control and relatively low power consumption.

Embodiments of the device may include a variable suction controlled by the user or another remote operator. A user can select a print remotely and the unit will switch to that pressure within seconds. The unit may include on board a pump that maintains suction and / or goes up / down from this initially established suction. Certain diaphragm pumps can be used as on-board pumps. Further, the motor that drives the diaphragm pump may be used to generate vibratory motion. In certain embodiments, the on-board pump may be a modified voice coil designed to mimic the actions of the diaphragm pump. The onboard pump may alternatively be accomplished using a voice coil actuator that moves a diaphragm in a sealed and valved chamber.

In embodiments using an on-board pump, or in embodiments using a remote-controlled pump, the suction may be programmed to match the vibratory motion of the motors or the macroscopic movement of the stimulators in the device. The vibration-driving algorithms described herein are adapted to the vacuum pumping system to provide fast reaction times and physically differentiable levels of suction to the clitoris. Further, certain embodiments use simultaneous or sequential suction waveforms or algorithms and vibration waveforms or algorithms to enhance the effect of the device.

In some embodiments of the device, variations of the stimulation parameters are particularly useful for providing the desired results to the user. For example, the stimulators may be varied between a high force level and / or a high frequency level and a relatively low force setting and / or low frequency settings. In the case of coin cell-type stimulators, power and frequency are coupled so that driving the high-frequency stimulator also drives the stimulator with a high force. To achieve the preferred variations in stimulation, coin cell-type stimulators can be switched between a high threshold of force and a low threshold of force. In the case of voice-coil type stimulators, power and frequency can be decoupled so that for a given force, the stimulation can be driven at any frequency. Without being bound by any particular mechanism or mode of action, it is believed that the relatively large variations in force or intensity of stimulation will produce a desirable user experience.

One of the advantages of the embodiments of the invention with multiple stimulators and suction patterns is that different parts of the anatomy can be stimulated at different frequencies. For example, different parts of the frenulum can be stimulated at different frequencies. It is generally understood that different types of nerves are stimulated to different degrees at a given rate, and that different nerves are more fully stimulated at different frequencies. One of the advantages of certain embodiments is the ability to deliver the appropriate rate and intensity of stimulation and / or suction to different parts of the vaginal anatomy. For example, of the three stimulators positioned as shown, the middle stimulator predominantly stimulates the tip of the clitoris and the right and left stimulators each stimulate the right and left corpora limb (and / or frenulum). The device may also enable the user to select and / or adjust the desired frequency for their anatomy and nerve distribution, thereby adjusting the experience of the user.

In certain embodiments, it is desirable to reduce the suction. For example, the edge of the suction cavity may be withdrawn, pushed or manipulated to create a leakage path. Furthermore, a valve connected in line with the suction pipe can be manually operated by the user to reduce suction. In embodiments using an onboard lift pump, the pump may be configured to be a constant one Therefore, if the pump stops, the unit will automatically shut down if there is a leakage path that the pump overcomes. Further, the device may be configured with a button by pushing the user, which opens a valve in the pump to relieve suction. Furthermore, the valve needed for the suction pump may normally be open. When power is delivered, the valve closes and completes the seal. However, when the force ends, the valve will open and the device will automatically degrade suction.

Certain embodiments of the present invention are designed and configured to increase blood flow in the vaginal tissue to promote blood flow to the clitoris and external genitalia while simultaneously applying stimulation to the clitoris and / or other vaginal tissue. The clitoris is a sexual organ filled with capillaries that deliver blood to a high concentration of nerves. Certain embodiments increase blood flow to stimulate the clitoris and enhance a woman's sexual response.

In women with symptoms ranging from lack of sexual satisfaction to sexual dysfunction, devices may provide certain embodiments: (i) increased genital sensation; (ii) improved vaginal moisturization; (iii) improved sexual satisfaction; (iv) improved sexual desire; and / or (v) improved orgasm. Certain embodiments of the invention are intended and configured to be used to treat women with reduced (i) agitation, (ii) moisture; (iii) sexual desire and or (iv) ability to achieve orgasm.

Certain embodiments of the invention are intended and configured to be a portable device designed to increase sexual satisfaction. Certain embodiments of the invention are intended and designed to be used as a "conditioning product" to prepare the user for a sexual event. Certain embodiments may be: use to help a woman prepare her body for a sexual experience, typically using 5 to 30 minutes before sex; Wearing during a sexual experience with a partner, including sexual intercourse; Use by a woman alone for recreational purposes to achieve orgasm; Use as an application, typically using a few minutes per day, to help facilitate more intense and enjoyable experiences during sexual intercourse with or without a partner; or use over time to help train the body to achieve a better natural sexual response.

The device 200 is placed over the clitoris by a woman, her partner or doctor ( to ). Gentle suction allows the product to stay in place (so it does not need to be held with your hands once placed), although it can be removed quickly and easily if desired. A woman can while she is the device 200 Wearing, sitting, getting up and walking around. As in shown is a small remote control 1550 or a smartphone app that uses the vibration intensity and the unique petting patterns of the device (such as counterclockwise movement, as in to pictured). The sequence can be customized in advance, and a "playlist" can be created. Once in place, the device offers 200 Silently hand-free sexual stimulation of the clitoris region in collaboration with a woman's body to help improve sexual response. Certain embodiments are small (about 1.5 inches long, about 1 inch wide), silent, waterproof and discreet. The product is latex free, hypoallergenic and washable with soap and water. It can be quickly and easily placed on the body, and it can be easily removed. It can be worn under clothing without anyone knowing that the user wears it. Being a hand-free product, the user can easily move, stand or walk while wearing the device for a few minutes a day while doing something else to help the woman's body maintain a higher level of sexual responsiveness to obtain.

to illustrate user interfaces for a smart remote control 1550 , The user interfaces provide means for controlling vibration and suction patterns, including pre-loaded patterns, user-configurable patterns, or combinations thereof. illustrates a user interface including a vibration on / off button 1551 , a vibration pattern selector 1552 , a vibration intensity selector 1553 and a vibration cycle speed selector 1554 , The vibration intensity selector 1552 and the vibration cycle speed selector 1554 are each shown with a numerical indicator in addition to a slider. The vibration pattern selector 1552 can be loaded with preloaded patterns, or it can be used to store user-configurable patterns. The user interface provides intuitive and easy-to-use means to control the vibration and suction patterns of the device.

and illustrate a user interface including a suction on / off button 1556 , a suction level selector 1557 and a Saugwechselgeschwindigkeitswählähler 1558 , The suction on / off button 1556 can also include an "alternate" section setting. illustrates that when the suction on / off button 1556 is in the "on" or "off position", the suction level selector 1557 has a single shift point, and the Saugwechselgeschwindigkeitsauswähler 1558 not available for use. If the user uses the suction on / off button 1556 on "On", the suction level selector can 1557 can be used to set a suction level at the device, and this suction level can numerically in units such. For example, "Target Hg" should be displayed.

illustrates a user interface where the suction on / off button 1556 was also set to "alternating". In the "alternating mode" the suction level selector has 1557 two slider points, and the suction rate selector 1558 is available. The "Alternate Mode" allows the user to set a primary suction level with the first spool point, and a higher suction level with the second spool point. The device may then alternate between these two levels of suction at a particular rate of alternation set by the user using the suction cycle speed selector 1558 , Thus, the user can control both the difference in suction levels and the speed at which the device alternates between the two levels of suction. Further, the user interface may include means for the user to store the two suction levels and the suction rate of change. The user interface may include pre-loaded suction change levels and speeds, user-adjustable suction change levels and speeds, or combinations thereof.

to illustrate views of a portion of particular devices having different tissue contacting configurations. In each of to For example, the inner components, such as the parts that comprise the vibration motors, are visible because the outer shell of the device bodies has been removed. shows the device with a relatively steep curvature along the tissue-contacting side of the device. That means the curvature of the sealing flange 225 from its approximate midpoint to the backside section 225R of the sealing flange 225 has a larger curvature than the same section of other parts of the device, which in the . and are shown. Furthermore, the sealing flange has 225 of in a relatively lower section (the section is described as lying below due to its placement when used below the clitoris) or a backside section 225A , This relatively longer section below (or back section 225R ) is configured to correspond to the anatomical curvature below the clitoris and to the interaction between the sealing flange 225 and to allow tissue. The upper and lateral flange portions are shorter relative to the longer distal flange portion to allow better positioning relative to the clitoris and to reduce interaction with the labia majora. For some users, this curvature will improve the fit, comfort and reliability of the suction attachment of the device. Other users may think that the curvature of the devices is as in . or pictured, is preferable.

The parts of the device that are in and can be illustrated from a molded part 22 be formed. The single molded part 22 closes the sealing flange 225 and upper parts connected to the apparatus body. Illustrates a perspective view of the device, showing the single molded part 22 attached to the body of the device 210 is attached to form the device. The upper parts of the single molded part 22 are inside the device body 210 positioned so that the vibration motors and the suction inputs to the control mechanisms within the device body 210 can be attached.

In some embodiments of the device, a removable flange assembly is provided. The flange assembly is connected to the device body and is removable from the device body. and show top views of the device 200 with the attached, removable flange assembly 225 ' , shows a variation in the width of the flange surface 223 '; in this case, the flange surface is 223 ' continue on a part of the device that is placed below the clitoris. As described herein, some embodiments of the invention include removable flange assemblies that may have a variety of geometries, curves, and configurations.

shows a perspective view of a removable flange assembly 225 ' , which is detached from the device body. shows a removable flange assembly hinge component 229 ' integral with the removable flange assembly 225 ' is. The removable flange assembly joint component 229 ' is connected to the device body and provides a substantially airtight seal with the suction chamber to allow operation of the device. Removal of the flange assembly may allow for a custom fit. This means that the user can choose from a selection of removable flange assemblies that have different dimensions, configurations, Materials, coatings and / or textures and combinations of these features.

For example, the width of the sealing flange 223 ' the removable flange assembly 225 ' be varied from a relatively narrow width to a relatively wide width. As another example, the curvature of the sealing flange may be varied from a relatively steep curvature to a relatively flat curvature. Further, a sealing flange on a single removable flange assembly may have a combination of widths and curvatures on its sealing flange. In yet another example, the removable flange assembly may be made of a combination of materials or of a single material having different properties. For example, the sealing flange may be relatively softer and more flexible (e.g., 0030A durometer silicone) while the removable flange body may be relatively stiffer (e.g., 0020A durometer silicone). A relatively stiffer removable flange body can help connect the immovable flange to the body of the device. In yet another example, the removable flange assembly sealing flange may have a variety of textures and coatings (such as a moistening or pre-moistening coating) that potentially improve the comfort, fit and / or reliability of the seal between the device and tissue.

For example, show to various embodiments of the sealing flange assembly 225 ' , to show the flange assembly 225 ' which is made of a combination of materials. The sealing flange 225 is a relatively softer and more flexible material, while the flange body 228 , which is connected to the device body, is relatively stiffer. The sealing flange part and the flange body part are formed together. In the embodiment of has the sealing edge 226 a sharper corner, so that when tissue is sucked into the suction chamber, this makes a tight turn with respect to the sealing surface 223 ' makes to create a seal on the sealing edge.

For some fabric types and geometries, additional features help create a seal either at the sealing edge or along the seal surface. In the embodiment of has the sealing edge 226 an additional rib, so that when tissue is drawn into the suction chamber, this a tight curve with respect to the sealing surface 223 ' and, when the tissue is undergoing a rush of blood, expands beyond the additional rib of the sealing edge to create a tight seal with the tissue and a mechanical barrier that helps prevent removal of the device during use.

In the embodiment of the has the sealing surface 223 ' a lead 233 that's all along the sealing surface 223 ' runs, and a depression 235 all the way along the sealing surface 223 ' runs. The lead 233 is very soft and flexible to keep a tight fit over any hair or small wrinkles in the fabric that makes up the sealing surface 223 ' to form, to prevent a Saugverlust along this hair or this tissue. The depression 235 Provides a space for hair or tissue and also provides a space for extra lubricant to be filled in or over the hair or tissue. In the embodiment of are the lead 233 and the depression 235 with the additional rib of the sealing edge 226 the embodiment of the combined.

The embodiment of to has two tabs 233 ' and 233 '' all the way along the sealing surface 223 ' run, and a lead 233 ''' that only partially along the sealing surface 223 ' runs. The lead 233 ''' is on the other flange part of the sealing flange 225 which is part of the flange in contact with the vulvar tissue below the clitoris. The lead 233 ''' connects to the lead 233 '' to create a continuous seal. The projections 233 ' . 233 '' and 233 ''' are very soft and flexible to form a tight fit over any hair or small folding differences of the fabric. The double and triple configurations offer various options, a seal along the sealing surface 223 ' to form and maintain, if a sufficient seal is not along the sealing edge 226 is maintained.

As in the bottom view of and in the plan view of has shown each of the embodiments of the to several suction holes 237 in the flange membrane 227 ' , Some of the holes 237 are placed opposite the circumference of the suction chamber to allow a larger seal at the sealing edge and the sealing surface. The stimulators are in the suction chamber membrane 220 integrated (not shown in to ). The membrane pockets 239 in the flange membrane 227 ' fit together and take the stimulators in the Saugkammermembran 220 on. The flange membrane 227 ' and the membrane pockets 239 are thin so that maximum energy from the stimulators can be transmitted through the membrane to the tissue.

In some embodiments, the sealing edge has a waxy texture that is excessive Provides material to adapt to variations in the tissue surface. The period and amplitude of the shaft on the sealing surface will vary with the material selected for the sealing surface to promote a safe and leak-resistant seal. In general, the sealing flange is made as thin as possible while still maintaining sufficient durability.

In some embodiments, the underlying portion of the gasket edge may be configured with a seam, a line or weakness, a thinned section, or other feature that includes a knobbed motion at the tissue surface. A soft puff of the soft tissue may close leakage paths in the area where the below-located section of the sealing flange interacts with the inner labia. . . and show a sealing projection 221 on the sealing flange 225 , The sealing projection 221 provides a labia surface to seal against. More than a sealing projection 221 can be used, and the sealing projections can be in other places on the sealing flange 225 be localized. The sealing projection 221 may include a suction inlet connected to the suction system of the device to promote sealing of the tissue against the projection. . and show different cross sections of the sealing projection 221 ,

Without wishing to be bound by any particular mechanism or mode of operation, the flanges and flange assemblies of certain embodiments may provide one or more of the following advantageous properties: (i) smoothing the vaginal tissue below and in the region of the flange; (ii) distributing the engagement forces between the device and the vaginal tissue; (iii) providing physical features that can fit beneath the labia majora; and / or (iv) increasing the leak path from the suction chamber to the outside environment. Any of these beneficial properties can help provide a reliable, comfortable and customizable anatomical fit.

In certain embodiments, the outer rib portion 220E the suction chamber 220 and / or the inner part of the sealing flange 223 ' like the sealing edge 226 , the primary parts of the device that form a seal with the tissue. That means, until the seal between the outer rib part 220E the suction chamber and / or the sealing edge / inner part of the sealing flange 223 ' is substantially interrupted, the device can maintain a sufficient seal with the tissue. In these embodiments, the sealing flange provides the above advantageous properties to increase the seal and to form a reliable, comfortable and adjustable anatomical seat. This may be the case for integral flange and sealing edge devices, and for devices using a removable flange assembly.

and illustrate a removable flange assembly 225 ' including a flange diaphragm 227 ; the stimulators are in the suction chamber membrane 220 integrated, which remains attached to the equipment cover. The flange membrane 227 ' may be made of the same material as or a different material than the sealing surface 223 ' be formed. The flange membrane 227 ' may be relatively taut over the central opening of the removable flange assembly 225 ' be, or it can be relatively relaxed. The flange membrane 227 ' may be hood-shaped, planar or shaped to suit the geometry of the device. The flange membrane 227 ' may be ductile or yielding or relatively unyielding. The flange membrane 227 ' includes one or more perforations or holes. The flange membrane 227 ' may during the process of forming the removable flange assembly 225 ' be formed. For example, in some embodiments, the removable flange assembly is 225 ' a molded part, and the flange membrane 227 ' can be integral with the removable flange assembly 225 ' are formed as a comparatively thinner section that houses the interior of the removable flange assembly 225 ' spans. The flange membrane 227 ' may be formed with holes or perforations formed during the molding process, or the holes or perforations may be formed after the molding process. The holes or perforations in the membrane may be integral with the generation of the membrane (that is, the membrane starting material already has holes or perforations). In some embodiments, the flange membrane may be fixed in place after the remainder of the removable flange assembly has been formed. The flange membrane may be adhered in place using suitable techniques such as sticking, heat sealing and the like. The flange membrane may be any type of fabric or web material suitable for tissue contact.

The flange membrane contributes numerous beneficial properties to the removable flange assembly. For example, the perforations in the flange membrane are of such a size as to permit air flow through the membrane while reducing the likelihood of trapping tissue within the membrane perforation or allowing the tissue to be trapped in the suction inlet of the tissue. The presence of the flange diaphragm allows for larger openings in the motor membrane to assist in cleaning the device. In another For example, the flange membrane may further provide user customization by providing a selection of textures for interacting with tissue. Further, the flange membrane may have a selection of perforation sizes and / or patterns which may increase or decrease the suction applied to the tissue in connection with the suction mechanism of the device.

illustrates a side elevational view of a removable flange assembly 225 ' , and and show, respectively, a side elevation view and a perspective view of a cross-sectional view of a removable flange assembly 225 ' , In these views, the removable flange assembly hinge component is 229 ' depicted as a pit region. In this embodiment, this recessed region is connected to the outer rib of the suction chamber on the device body. In other embodiments, the removable flange assembly hinge member may be a protuberance that fits within the recessed region located on the device body. Other configurations of the removable flange assembly linkage component may be used as long as these configurations provide a substantially airtight seal with the suction chamber.

The removable flange assembly offers the advantage of improving the simplicity and reliability of cleaning the entire device. In some embodiments, the removable flange assembly is formed from materials that allow the removable flange assembly to be cleaned in a dishwasher while the remaining body of the device is simply rinsed or otherwise cleaned by hand. In such an embodiment, the tissue-contacting portions of the device may be cleaned more thoroughly than if the flange assembly were not removable. Alternatively, the removable flange assembly may be disposable and disposable. A device may be packaged with many removable flange assemblies, and these arrangements may be identical, or they may have a variety of different features. Further, a user may purchase other removable flange assemblies for use with the originally purchased device body.

Another advantage of the flange diaphragm is improved simplicity and reliability of cleaning the device body. In embodiments without a flange membrane, the flexible membrane of the suction chamber includes inputs that are configured and of such a size to reduce the possibility of tissue retention and injury. This means that the entrances are narrow and / or offset from the fabric. Small and / or remote inputs can be more challenging and thoroughly clean than larger inputs or non-remote inputs. Furthermore, the inputs 220H to the periphery of the suction chamber 220 be localized as in displayed. Such a place for the entrances 220H may improve the drainage of fluid from the device body after use or after cleaning when the device is placed with the edge of the suction chamber upside down on a surface. Typically, there will be at least one hole in the top center of the flange membrane to allow engagement with the stimulators.

Referring again to becomes the device body 210 Illustrated to give a view of the interior of the device body 210 to offer. The vibration motors 280 are inside structures in the single molded piece 22 positioned so that the stimulation from the motors can be effectively transmitted to the tissue, and parts of the vibration motors 280 are also reachable with the regulator block 215 to be connected. In this case is controller block 215 illustrated as a printed board. An onboard pump 135 is also in the device body 210 positioned. The onboard pump 135 is in fluid communication with the suction chamber to provide suction in that chamber and also in fluid communication with an exit. The exit is an outlet for air or fluid pumped out of the suction chamber and an inlet for air towards the suction chamber when suction is reduced. In some embodiments, the on-board pump sends 135 pumped air from the suction chamber via heat generating elements within the device body 210 before reaching the exit. Such airflow can help dissipate heat and provide safety and reliable use of the device.

In some embodiments, heat generation in the device may be monitored using a component such as a thermistor. Thermistors can be inside the device body 210 be positioned, or may be integral with the regulator block 215 be. When the thermistor senses a threshold temperature, it can turn off the power to the unit and / or blow external air into the unit to help cool the unit and then remove the suction.

In some embodiments, the onboard pump is controlled by the governor block via a closed feedback loop. That is, the controller block is configured to maintain a crowd pressure that can be adjusted by the user, or that can be loaded as part of a pre-programmed suction algorithm. To do this, the controller block reads real-time data from the on-board pressure sensor, which is configured to control the pressure within the suction chamber monitor (negative pressure in case of suction). Based on the real-time data, the regulator block may engage the on-board pump to draw a higher suction into the suction chamber, or may engage a check valve in fluid communication with the outlet to blow air into the suction chamber. After the device has generated sufficient suction to seal it in place to the user, in typical operation, the governor block will periodically put the on-board pump into service when suction is slowly lost due to leakage.

and illustrate views of the device 200 including a device body 210 , The sealing flange 225 is with the device body 210 connected. The curvature of the sealing flange 225 provides a comfortable and reliable anatomical seat. Furthermore, the front part has 225f of the sealing flange 225 a narrower profile than the back 225R of the sealing flange. This configuration allows the device body 210 to protrude over the user's pubic bone while the sealing flange 225 is in contact with tissue. The back part 225R of the sealing flange 225 is relatively expanded to provide another sealing surface, similar to FIG displayed. The relatively narrower front part 225f of the sealing flange 225 is configured to sit comfortably and reliably on the top of the labia majora.

and also illustrate device body 210 Configured to sit comfortably and reliably on a user in various contexts. How out can be seen, especially the back tapered 210r of the device body 210 against the sealing edge 225 of the device 200 , This rejuvenation can be helpful in allowing the partner to have access during vaginal intercourse. A device without such a taper could prevent access. As further out it can be seen, the rear part tapers 210r against a point in relation to the pages of device 200 , This rejuvenation can be helpful in allowing the user to stand and walk while the device is engaged. In a device without such rejuvenation, some users may experience release of the device when standing or walking due to contact with the thighs of the users. Furthermore, the mechanisms, the regulator block, batteries and other internal components can be directed towards the front of the device body 210 be positioned. Positioning the inner components in this manner may place the center of mass of the device in such a manner as to reduce the tendency of the device to fall off or disengage from the user. This means that if the center of mass of the device is also from the user side of the device, or in some cases towards the rear part 210r of the device body 210 , may cause the device to act as a lever and "peer" the device away from the user when the user is standing, or even when the user is lying down.

illustrates a perspective view of a device 2400 containing a device body 2410 , a sealing flange 2425 and an onboard manual pump 2435 includes. The onboard manual pump 2435 is in fluid communication with the suction chamber of the device. The pump 2435 is depicted as a bellows-type pump where the user pushes down on the outer surface, thereby expelling air from the pumping chamber through an outlet. The pumping chamber is in fluid communication with the suction chamber by means of one or more valves which allow suction to be drawn from the interior of the chamber, but prevent air from entering the pumping chamber when expelling air from the pumping chamber. Other manual pumps such as squeeze ball systems (similar to a blood pressure cuff) or piston systems may be used. The on-board manual pump may be secured in a flat profile state when the pump is not activated.

Certain embodiments of the invention include a device for promoting female sexual well-being and female sexual desire. Certain embodiments of the invention include a device for: (i) female sexual arousal disorders; (ii) treat hypoactive sexual desire disorders and / or (iii) female orgasmic disorders. Of course, the invention promotes a woman's own sexual response without unwanted, lasting side effects. A woman will enjoy sexual intimacy again and feel confident about her body's ability to respond to sexual stimulation.

In embodiments described herein, coin-type vibratory motors can be placed on the tissue side, in a planar configuration against tissue, or at an angle with respect to tissue therebetween. The angle with respect to tissue can provide a varying amount of intensity. In some embodiments, the device is configured so that the motor angle can be adjusted directly by the user (manually) or indirectly by selecting particular stimulation patterns from the controller.

illustrates an embodiment in which a body vibration source 211 (like a vibration motor) on the device body 210 provides a baseline level of vibration stimulation. The vibration on the device body 210 can, as described in more detail below, the result contacting the device body 210 be with a conventional vibrator. Alternatively, a body vibration source 211 on the device body 210 included in addition to any of the stimulation elements described herein for delivering stimulation to the vaginal tissue within a tissue chamber (or suction chamber). Advantageously, the body vibration source provides 211 a stimulation level that serves to effectively amplify the stimulation provided in the tissue chamber. This means that a baseline level of vibration can contribute to the blood rush and arousal process, and that the stimulation elements integrated into the tissue chamber also drive the blood rush and excitation process. Further, the internal vibration motors may be initially used for arousal, and then the body vibration source may be used as additional vibration for additional sensation and / or for achieving a climax. Furthermore, the baseline vibration of the body vibration source cooperates 211 with vibration motors to produce resonant and / or harmonic vibration patterns with the tissue. Certain users may prefer labia stimulation associated with clitoral stimulation, and the body vibration source 211 to provide labia vibration stimulation.

In related embodiments, as in Illustrated, the multiple body vibration sources 211 and 211b on the device body 210 be positioned. If several motors on the device body 210 The multiple body vibration sources can be positioned 211 . 211b be configured to vibrate at different frequencies to produce different vibration profiles. The vibration profiles may be in-phase, out-of-phase, two-phase (di-phase amplification generating), or multi-phase.

illustrates an embodiment of the device in which one or more stimulation sources (the vibration motors) 180a . 180b . 180c and 180d in a stimulation chamber 182 are included, and the stimulation chamber 182 is positioned in the device so that it can come into contact with vaginal tissue and in particular the clitoris. The stimulation sources 180a . 180b . 180c and 180d are free, in the stimulation chamber 182 to stimulate and / or vibrate, and thus periodically vibratory stimulation on a soil surface 183 the stimulation chamber 182 Apply with the suction chamber 120 connected is. The stimulation sources 180a . 180b . 180c and 180d may be connected to the regulator block by means of cables, but they may otherwise freely move within the stimulation chamber 182 move. In some embodiments, the control signals are wireless. Further, the motors may be driven and / or charged by RF signals so that they are not tied by cables. In this case, the stimulation sources 180a . 180b . 180c and 180d completely free in their movement within the vibration chamber. A feature of these embodiments is that the stimulation sources 180a . 180b . 180c and 180d not in the suction chamber 120 hang, but rather periodically into the suction chamber 120 penetration.

. and illustrate embodiments in which stimulation features 485 be designed to penetrate into the tissue chamber. to work in a similar way as the one in disclosed embodiments. For example, an array of pacing features 485 placed above the tissue chamber, and the assembly can be rotated or otherwise moved with respect to tissue. In some embodiments, as in shown can be another displacement element 486 above the array of pacing features 485 be positioned, and the movement of the displacement element 486 forces individual or groups of pacing features 485 in the order to penetrate into the tissue chamber. displacement element 486 and the stimulation features 485 can be permanent magnets or electromagnets, so that the displacement element 486 a movement of the stimulation features 485 generated by magnetic repulsion. In embodiments in which the stimulation features 485 are permanent magnets or electromagnets, can stimulation characteristics 485 be positioned in a receiving shaft or embedded in a membrane to keep the component separated. Without such a receiving well or a membrane, the magnetic attraction between the stimulation features could 485 make them bind together, preventing the desired movement. illustrates an embodiment in which an array of displacement elements 486 above an array of pacing features 485 is arranged. The displacement elements 486 are selectively drivable to generate stimulation patterns by stimulation features 485 be forced into the tissue chamber 220 penetrate.

In many of the embodiments described herein, it is advantageous to minimize the number of moving parts. It is also advantageous to minimize the number of relatively expensive parts. The embodiments employing an array of stimulation elements that are driven in a manner by relatively fewer motors, magnets, or other energy sources achieve the benefits of less moving parts and / or less expensive parts.

In another embodiment as in . and As shown, the vibration source closes a vibrating stylus 3250 one with a motor 3220 connected is. The stylus 3250 is within a translation framework 3200 positioned the stylus 3250 capable of being translated quickly to various positions with respect to the tissue in the tissue chamber (or suction chamber). In a preferred embodiment, the translation frame is 3200 configured so that the stylus 3250 moved back to the center within the frame when translation forces are removed. For example, the stylus 3250 by means of an elastic component 3330 with electromagnet 3340 get connected. The motor housing 3220 may include a permanent magnet or an electromagnet, which is actively translated by the fields generated by the electromagnets in the translation frame. The motor housing 3220 Alternatively, it can be moved by a disc-like system between movable supports of the transmission frame. The one with the stylus 3250 Motor connected may be in the vibration of the stylus 3250 and the translation framework 3200 be isolated by the engine on a damping structure, such as foam, is attached. More than a stylus 3250 and / or more than one translation frame 3200 can be used in various embodiments described herein. In some embodiments, the stylus 3250 used to stimulation characteristics 485 in an arrangement 48 to force such. B. shown in to penetrate the tissue as further described herein in other embodiments. further shows an embodiment in which the stylus 3250 by the interaction of a magnet 3255 which is positioned on the stylus arm, is translated. electromagnets 3253 and 3257 are used to the stylus 3250 translate and engine 3220 vibrates the stylus 3250 ,

In embodiments of the device, as in and illustrated, is an engine 3580 outside the suction chamber 3590 localizes and is connected or otherwise communicates vibration at a connection 3530 that are at least partially within the suction chamber 3590 is appropriate. The connection 3530 interacts directly or indirectly with tissue within the suction chamber via a stimulation feature 3520 , For example, the connection 3530 Stimulate tissue directly by making contact with the tissue, or the compound 3530 can indirectly stimulate tissue by mediating vibration to a stimulation component (such as an array) 487 , shown in or as shown in ), which is in contact with tissue. The stimulation component 3520 like that in pictured, may have one or more protrusions 3572 that stimulate tissues directly. The projections 3572 may have a range of stiffnesses to produce a variable stimulation profile. For example, some projections 3572 be relatively flexible, and others can be relatively stiff. The rigid protrusions transmit relatively more vibration than the flexible protrusions.

In some embodiments, the suction chamber includes gripping members connected to and driven by a motor on the outside of the suction chamber. As in a schematic view in shown, one or more gripping organs 3630 selectively by one or more motors 3680 be addressed. That means an individual engine 3680 one or more gripping organs 3630 can move or vibrate as dictated by a controller. Further, the controller may be the individual engine 3680 pretend, just a gripping organ 3630 or to move or vibrate several gripping organs. If the individual engine 3680 is given, several gripping organs 3630 To move or vibrate may be the engine 3680 Furthermore, be given with which sequence the multiple gripping members 3630 to move or vibrate. illustrates a coupler 3650 that is between each engine 3680 and certain gripping organs 3630 is positioned to selectively transmit the vibratory motion of the engine 3680 to the desired gripping member or the desired gripping members 3630 to enable. The coupler can selectively transmit motion or vibration, for example, by means of magnetic coupling and mechanical coupling. For example, the gripping organs 3630 by selectively activating an electromagnet to connect a permanent magnet to a proximal end of a gripping member 3630 to pull and with the coupler 3650 connect to. Then, with rotation of the polarity of the electromagnet, the gripping member 3630 be decoupled and return to its original position. In another, in shown example, one or an array of grippers 5655 the near end of a given gripping organ 3630 to enable transmission of motion or vibration, and can be released to stop the transmission of motion or vibration. As with other embodiments described herein, the gripping member 3630 be translated into two dimensions, as in shown.

Advantageously, in some embodiments, multiple motors may be arranged in a layered configuration with tie bars of various lengths. This is an advantage because multiple motors can be arranged in a relatively small space and can transmit vibration to a larger vibration member. Such an arrangement can also with a Stimulator can be connected, such as a vibration motor that hangs within the suction chamber. Alternatively, the multiple motors may be layered and / or configured to transmit vibration in a relatively high resolution. This means that the motors communicate by means of rods, z. B. to a vibrating element whose base is relatively smaller than the base of the engine configuration. Furthermore, the vibration element can have a high density of stimulation elements which can be addressed individually or repeatedly by the motors.

In contrast to some prior art devices, these embodiments interact directly with a stimulation device having an array of protrusions. That is, some prior art devices simply shake an entire array of protrusions rather than provide a series of transfer points that efficiently transfer vibration from an engine to a demarcated portion of a stimulation assembly.

In some embodiments, the motor or motors may be located separately from the stimulation and / or suction chamber so that the motors are contained in a separate housing. The motors can transmit vibration to the site of stimulation by means of a cable or rod assembly or other similar components. The motor housing may be mounted on a garment or other portable object. Or the motor housing can be placed close to the user without being worn or held directly by the user.

and illustrate an embodiment in which a single motor 4050 a stimulation coupling element 4000 drives, which has surfaces of different stiffness. Stiff surfaces of the stimulation coupling element 400 can swing harmoniously or resonantly with the engine 4050 , Thus, a single engine 4050 drive a spatially delimited vibration stimulation.

The stimulation coupling element 4000 can be a network of relatively stiff nodes 4010 be that by relatively stiff spokes 4020 are connected. The stimulation coupling element 4000 can also be less rigid regions 4300 which help to isolate the vibration to the nodes. That means the presence of less stiff regions 4030 serves to help the surfaces resonate or harmoniously with the drive motor 4050 vibrate, spatially separate.

Alternatively, the nodes 4010 Include passive actuators that can connect to the drive motor to provide spatial limited stimulation. A passive actuator may include a piston and cylinder configuration that stores energy, such as by a spring or equivalent, and the stored energy may be released and recharged by resonant coupling of the node 4010 with the drive motor 4050 , In some embodiments, the passive actuator may be at the nodes 4010 be selectively controlled by activating and deactivating local dampers. For example, passive actuators have selectively controllable shutter mechanisms. Such mechanisms can be electronically controlled by a device control block that provides patterns for spatially limited stimulation. Technology of micro-electrical mechanical systems (MEMS) provide routes for local selective response control of active and passive actuators and may be implemented in the embodiments described herein.

The devices described herein are advantageously attached to the user's body. In some embodiments, the commercial chamber is configured to sit under the outer labial lip such that the device is portable without any other attachment mechanism (although suction is an optional attachment mechanism). In some embodiments, additional features on the device provide additional ways of conveniently backing up the device. For example, adhesives (such as rubbery, sticky, or otherwise adherent materials) may be applied to the tissue flange of the device. Furthermore, flexible wings can 294 , as in shown, removable on the device body 210 be present (as seen from the ground), and the wings 294 can be configured as pressure-sensitive, temperature-sensitive or moisture-sensitive surfaces. A machine 200 can be supplied to the user with several attachable and disposable adhesive wings 294 to be delivered. For many users, it is beneficial to apply an adhesive to the area above the clitoris, as in the clitoral wrap, where the tissue is more skin than mucosa.

The lateral projections 292 on the sides of the device 200 , as in Shown in cross-section may be used to provide a safe and comfortable attachment. Such lateral projections 292 correspond to the fabric flange 225 which extends below the labia majora. The lateral projections 292 can be compliant and flexible to allow placement. Furthermore, the lateral projections 292 be configured to curve or snap in place after the tissue flange 225 has been placed under the outer labia. The lateral projections 292 can be configured to vibrate to the outside Labia for a user interested in such additional stimulation to pass. Alternatively, the device may include soft clips for securing the device to the external labial lip.

Alternatively, the soft and relatively adaptive extensions can 293 be used to provide a secure and comfortable attachment to the lower part of the device 200 are attached, as in (seen from the ground) and 52D (an isometric view). These lower processes 293 are configured to expand under the lip fold and press laterally to the device 200 to stabilize. The extensions 293 can be pliable and flexible so that they can be compressed during device positioning, allowing them to expand again and provide gentle support for the device.

In some embodiments, the system includes 4100 an intravaginal unit 4160 One with a clitoral stimulation device 4110 connected is. The intravaginal unit 4160 may provide stimulation, including all types of stimulation disclosed herein. Additionally or alternatively, the intravaginal unit 4160 Include any component of the system disclosed herein. Alternatively, the intravaginal unit 4160 Be passive and act as a single unit for extra compression / stabilization for the clitoral stimulation device 4110 to offer. For example, in some embodiments, the intravaginal unit includes 4160 a motor with stimulation elements in the clitoral stimulation device 4110 connected is. The motor can be configured to provide both intravaginal vibration and clitoral stimulation by transmitting vibration through the stimulation elements. A transmission element, such as a cable, connects the motor in the intravaginal unit 4160 with the clitoral stimulation device 4110 , The intravaginal unit 4160 may be configured to indicate and stimulate an erogenous zone or erogenous zones on the anterior vaginal wall ("G point").

The connection between intravaginal unit 4160 and the clitoral stimulation device may be a "C-shaped" connector 4150 which is configured to provide a safe and comfortable fit. For example, the connector may be reversibly deformable, or it may be capable of bending open and closing on return to an original position. The connector 4150 can be formed from a compliant or stretchable cable that is enclosed in a protective cover. The connector can be a hinge point 4155 have to allow a placement. The intravaginal unit 4160 may be configured to vibrate or otherwise stimulate the G-spot by means of a stimulation source (such as a motor) located near where the unit is located 4160 the connector 4150 meets. In another aspect, the stimulator may be for the intravaginal unit 4160 in the housing of the clitoral stimulation device 4110 be localized.

In some embodiments, the intravaginal unit is not physically connected to the clitoral stimulation device. In such embodiments, the intravaginal unit may communicate by near-field radio frequency technology or other intermediary device communication. In such embodiments, where the intravaginal unit is not physically connected to the clitoral stimulation device, the intravaginal unit may still provide vibratory stimulation or other stimulation by means of the stimulation elements included in the intravaginal unit.

An intravaginal unit can be used to provide clitoral stimulation by vibration or vibration with a relatively small device applied to the clitoris. Advantageously, such embodiments may use a soft clip or similar device applied to the clitoris, and the soft clip may be driven to provide stimulation by the intravaginal unit. In one embodiment, the soft clip includes permanent magnets or electromagnets that can be driven to compress and disperse to provide stimulation to the clitoral tissue. An intravaginal unit or separate unit can provide the external magnetic field used to drive the soft clip.

Other embodiments of the device, as in . . and shown, place some or all of the stimulators below the clitoris. The body 4510 of the device 4500 In these embodiments, it is placed in the space between the lips so that the center of mass of the device is further below than in the other embodiments described herein in which a significant portion of the device remains on the pubic mound. An advantage of this embodiment is that the weight of the device is below the clitoris, and thereby a secure and comfortable attachment can be provided. The device may partially occlude the urethral opening and / or the vaginal opening. The device may be configured to take advantage of its position and may use any of the intravaginal unit embodiments described herein. Another advantage of this embodiment is that the stimulators 4580 can contact the clitoris directly without clitoral To be dependent on blood. This means that by placing the motors below the clitoris, the motors can contact the clitoris when it is in a relatively limp state. . and Illustrate a front view, a perspective view, and a side cross-sectional view of the clitoral engagement chamber, respectively 4550 ,

In certain embodiments, the suction chamber is flexible and / or capable of expansion. The suction chamber is brought into contact with clitoral and / or vulvar tissue. When suction is applied, tissue is captured and the flexible suction chamber displaces tissue and optionally expands to capture additional tissue and delivers the tissue to stimulation elements such as vibratory motors. In these embodiments, the vibration motors may be located outside of the suction chamber, as opposed to hanging in the suction chamber. Furthermore, clitoral and / or vulvar tissues may be gently pushed against the stimulation element in addition to or instead of being sucked to the stimulation elements. By pressing tissue z. For example, the walls of the suction chamber may be plastically deformable so that the chamber can be manually manipulated by a user to squeeze tissue. In another example, the suction chamber walls may be made to collapse and the user may manually separate them while placing on the clitoral and / or vulvar tissue.

In some embodiments, electromagnetic actuators configured differently than conventional voice coils are used. For example, planar magnetic donors can be used as actuators to deliver stimulation to clitoral and / or vulvar tissues. Planar magnetic donors can provide direct mechanical stimulation through a diaphragm or membrane that directly contacts tissue, or they can provide acoustically mechanical stimulation that drives air against clitoral and / or vulvar tissue.

Planar magnetic encoders typically consist of a diaphragm having a printed circuit scale across the surface of a thin film substrate and a magnetic assembly. The magnetic arrangement creates a magnetic field parallel to the diaphragm. The thin diaphragm is highly responsive to electrical signals and can be used to create spatially delimited kinesthetic sensations and forces.

In other embodiments, magnets may be embedded in a thin membrane positioned and configured to stimulate clitoral and / or vulvar tissue. An electromagnetic array may be positioned over the membrane to drive specific magnets and create spatially limited stimulation. This means that selective activation of the electromagnetic array can drive individual or groups of embedded magnets. Alternatively, instead of an electromagnetic arrangement, one or more movable permanent magnets may be used to selectively drive individual or groups of embedded magnets. The permanent magnet may be moved by a variety of mechanical or electromechanical means according to various programmable or pre-programmable patterns.

In certain embodiments, the system includes a vacuum reservoir. That is, the system includes a chamber capable of holding a negative pressure that can be applied to the suction chamber of the device through a valve system. During the initial attachment, after reaching the desired suction level in the suction chamber, z. B. by means of an on-board pump, the vacuum source continues to run to provide the vacuum reservoir with an excess negative pressure. The on-board pump may stop running, and if a small leak develops, the negative pressure in the vacuum reservoir may provide suction to the suction chamber until exhausted, and then the pump may be turned back to fill the reservoir and suction chamber to then stop running again. An advantage of the vacuum reservoir is that the desired suction level can be maintained while the suction source is less run than a system without a vacuum reservoir.

Systems described herein can be equipped with sensors and reading capabilities. The data collected from the reading can be used in a variety of ways, e.g. B. for presentation to the user and / or feedback to the device control systems. Read parameters include tissue temperature, tissue resistance, blood flow, tissue swelling and / or blood rush, heart rate and blood pressure. The data can be displayed on the user control device, such as a smartphone. The data may be displayed graphically and / or numerically and may be applied via a visual representation of the anatomy. Significantly, the data presented may be presented in an "excitation meter" that provides information to the user. Further, the status of the user's arousal may be used to provide a bio feedback loop to control the device. For example, the user may set an excitation level on the device before use, and the device may Monitor the user's excitation status. By reading the excitation status, the device control system may increase or decrease the stimulation to match the user-specified status.

In some embodiments, actuators are used instead of coin or other vibratory motors. One type of actuator is a linear actuator in which a component is driven back and forth. The electromagnetic voice coils described herein are an example of a type of linear actuator wherein a diaphragm is driven in response to an electromagnetic coil. Other linear actuators include electromagnets and passive magnets arranged in a piston-like configuration to produce linear motion.

In certain embodiments, the actuators used are driven not only or not at all by electromagnetic fields. For example, pneumatic actuators may be used in which a reservoir of compressed gas (including air) is charged by means of a pump. The pump may be a manual pump, such as a bellows or syringe pump. The linear actuator of the pneumatic actuator may be biased in a first position and then driven to a second position by an outgass of gas released from the reservoir through a valve system. Other configurations of pneumatic actuators are useful in these embodiments.

In certain embodiments, miniature scale actuators of other types are used to generate stimulating forces. For example, various types of thermo-mechanical and thermoelectric actuators can be used to drive stimulating elements in a device. Such actuators include those that use thermoelectricity to expand a fluid, and such fluid expansion can drive a mechanical element (eg, a piston). Other thermoelectric actuators, which may be useful in some embodiments, include shape memory alloys, such as. Nitinol, which can be used to produce a mechanical movement in thermoelectric heating. Generalized are actuators capable of producing kinesthetic forces and sensations applicable as stimulators, including the types of actuators disclosed herein.

In some embodiments, pneumatic systems may be used to provide stimulation. Miniature input pneumatic systems can provide fast puffs (or other gas) to produce tactile sensations and / or kinesthetic sensations and forces. The rate and volume of the breezes can be varied to produce a variety of stimuli. Multiple inputs for delivering puffs can be used to achieve spatially delimited clitoral and / or vulvar tissue stimulation. Multiple inputs can be configured to use a valve and input assembly that delivers air from one or more pneumatic sources. Alternatively, an array of pneumatic sources may be used.

In some embodiments, circulating air may be used to provide stimulation. As with the air pulse or draft, a pneumatic source or pneumatic sources can supply air through a valve and input system. Unlike a pulsed air system, a system of circulating air can be used to stimulate tissue by blowing across the tissue rather than pulsing against the tissue. Certain embodiments use both types of pneumatic systems in which air is circulated and pulsed. Furthermore, pulsed air may also be directed across the surface of a tissue. And pneumatic stimulators may be used in conjunction with any other stimulation types disclosed herein.

Further, referring to systems including multiple valves and inputs, in some embodiments, a source of suction is used to apply suction through a valve and input assembly. Such a system may engage clitoral and / or vulvar tissue at multiple spatially defined locations. Alternatively, multiple and separately controlled suction sources may be used in conjunction with or in lieu of an array of valves and inputs. In some embodiments, rapid suction fluctuation may be used to produce kinaesthetic sensations and forces.

In many of the embodiments described herein, it may be desirable to apply therapeutic energy to the clitoral and / or vulvar tissue, such as, e.g. As light energy or electromagnetic energy. Certain frequencies of light can reduce tissue inflammation and certain frequencies of light can increase local blood flow.

In many of the embodiments described herein, it is desirable to provide ambient sounds by means of the device or system. Ambient sound can be a background noise that promotes feelings of well-being and / or arousal in the user. In addition, the ambient sound may be a "white noise" that provides a relatively constant background sound, thereby masking or reducing sounds produced by the device during operation. In this regard, the device or system may include an active noise cancellation system.

While the invention has been described with reference to the specific embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the scope of the invention. In addition, modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from its scope. Therefore, it is intended that the invention not be limited to the particular embodiments disclosed, but that the invention include all embodiments falling within the scope of the appended claims.

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited non-patent literature

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• Read S., King M., Watson J .: Sexual Dysfunctions in Primary Medical Care: Dissemination, Characteristics, and Evidence by the General Practitioner. J. Public Health Med. 19: 387-391, 1997 [0003]
• Laumann E., Paik A., Rosen R: Sexual dysfunctions in the USA, incidence and influence values. JAMA, 1, 281: 537-544 [0003]
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Claims (28)

A device for promoting sexual arousal in a female user, comprising: a tissue-contacting chamber including a suction chamber; and at least two stimulators that are at least partially flexible within the suction chamber. The apparatus of claim 1, further comprising a suction adapter, wherein the suction adapter is in fluid communication with the tissue contacting chamber. The device of claim 1, wherein the parameters of the stimulators are controlled, and the parameters are selected from the group consisting of vibration frequency, vibration intensity, vibration duration, sequence of engine vibration, and combinations thereof. The device of claim 3, wherein the stimulators are controlled by selection from a pre-programmed algorithm, a user-customizable algorithm, or combinations thereof. The device of claim 1 comprising a portable device body having an attached portion that fits between the labia majora below the clitoris and a housing that exits the labia majora above the clitoris, the attached portion having a length and the housing having a height who allow sexual intercourse. The device of claim 5, comprising three stimulators in a triangularly spaced relationship forming a cavity for the clitoral tissue. The device of claim 1, wherein the stimulators are coin-type miniature motors. Apparatus according to claim 6, wherein the coin-type miniature motors are enclosed in a convex membrane. The device of claim 1, comprising a suction generating device and a portable device body, wherein the suction generating device is detachable from the portable device body. The device of claim 9, wherein the stimulators remain substantially in contact with tissue after the suction generating device is removed. The device of claim 1, further comprising a membrane at least partially enclosing at least one of the stimulators. The device of claim 11, wherein the membrane is connected to the chamber. The device according to claim 12, wherein the stimulators are flexibly suspended by means of the membrane. The device of claim 11, wherein the membrane is arranged to be displaced by the clitoris of the user. The device of claim 1, wherein the stimulators are controlled so that the user experiences a simulated macroscopic movement. The device of claim 1, wherein the vibration generated by a stimulator is isolated from a wall of the tissue contacting chamber. The device of claim 1, wherein the stimulators are motor-type stimulators and are individually controlled. A device for promoting sexual arousal in a female user, comprising: a tissue-contacting chamber including a suction chamber; wherein the suction chamber is in fluid communication with a suction pump; and wherein at least two stimulators are mounted within the suction chamber; wherein the motors and the suction pump are adapted to be independently controlled by means of a control circuit. The apparatus of claim 18, further comprising a regulator block, wherein the regulator block includes previously loaded vibration patterns and previously loaded suction patterns. The apparatus of claim 19, wherein the controller block is configured to allow the user to create vibration profiles and suction profiles. The device of claim 18, wherein the device comprises a portable device body, and wherein the suction pump is mounted within the device body. The device of claim 18, wherein the stimulators are motors. A device for promoting sexual arousal in a female user, comprising: a tissue-contacting chamber; and at least two stimulators connected to the chamber, wherein the stimulators are positioned so that the user experiences spatially delimited stimulation. A device for promoting sexual arousal in a female user, comprising: a tissue-contacting chamber; and at least two stimulators connected to the chamber, the stimulators being controlled so that the user experiences spatially-limited stimulation. Apparatus for stimulating clitoral tissue, comprising: a mechanically stabilized housing; a suction chamber within the housing, and a plurality of transmitters connected to the suction chamber. A device for promoting sexual arousal in a female user, comprising: a mechanically stabilized and portable housing; and a stimulating surface comprising at least one electroactive material, wherein the electroactive material is configured to produce macroscopic stimulation. A device for promoting sexual arousal in a female user, comprising: a tissue-contacting chamber including a suction chamber, said suction chamber being in fluid communication with a programmable suction pump; and at least two stimulators mounted within the suction chamber, and wherein the motors and the suction pump are adapted to be independently controllable by a control circuit. Apparatus as substantially described herein, with reference to and as explained by the accompanying drawings.

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