WO2025010282A1 - Disposable furlow insertion device with collapsible pusher - Google Patents
Disposable furlow insertion device with collapsible pusher Download PDFInfo
- Publication number
- WO2025010282A1 WO2025010282A1 PCT/US2024/036581 US2024036581W WO2025010282A1 WO 2025010282 A1 WO2025010282 A1 WO 2025010282A1 US 2024036581 W US2024036581 W US 2024036581W WO 2025010282 A1 WO2025010282 A1 WO 2025010282A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pusher
- end portion
- slot
- elongate member
- insertion device
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/34—Trocars; Puncturing needles
- A61B17/3468—Trocars; Puncturing needles for implanting or removing devices, e.g. prostheses, implants, seeds, wires
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/26—Penis implants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/06—Measuring instruments not otherwise provided for
- A61B2090/061—Measuring instruments not otherwise provided for for measuring dimensions, e.g. length
Definitions
- This disclosure relates generally to devices for insertion of bodily implants and, more specifically, to disposable insertion devices for bodily implants, such as penile prostheses.
- One treatment for chronic, organic, male erectile dysfunction is the implantation of a penile prosthesis that mechanically erects the penis.
- Such prostheses can have different physical constructions (e.g., materials, mechanical structure and function, etc.) and configurations (e g., physical dimensions, etc.).
- a penile prosthesis can be in the form of a cylinder (e.g., malleable, inflatable, etc.) that is selected based on the physical requirements of an intended recipient (a patient).
- an appropriate penile prosthesis can be implanted within a corpus cavemosum (corpus cavernosa) of a patient’s penis by medical personnel that are trained and knowledgeable regarding the implantation and use of penile prostheses.
- Insertion devices can be used to facilitate the insertion of a penile prosthesis into the corpus cavemosum of a patient.
- Such Furlow insertion devices can be used for measurement of an insertion length within the corpus cavernosum, as well as for facilitating insertion of a penile prosthesis by deploying a suture-carrying needle, where the needle and/or suture are used to introduce (draw, pull, insert, implant, etc.) the prosthesis into the corpus cavemosum.
- an insertion device includes an elongate member defining a lumen extending from a first end of the elongate member to a second end of the elongate member, and a pusher having a first end portion.
- the first end portion of the pusher is configured to be disposed within the lumen defined by the elongate member and move from a first position within the lumen defined by the elongate member to a second position within the lumen defined by the elongate member.
- the first end portion of the pusher defines a slot.
- the first end portion of the pusher defines a receiving portion. In some implementations, the first end portion of the pusher defines a receiving portion configured to receive a portion of a needle. In some implementations, the pusher has a second end portion opposite the first end portion, the second end portion includes a handle portion. In some implementations, the pusher has a second end portion opposite the first end portion, the second end portion includes a handle portion, the handle portion being configured to extend from the lumen defined by the elongate member.
- the pusher has a second end portion opposite the first end portion, the second end portion includes a handle portion, the handle portion being configured to extend from the lumen defined by the elongate member while the first end portion of the pusher is disposed within the lumen defined by the elongate member.
- the slot defined by the first end portion of the pusher extends in a direction parallel to a longitudinal axis of the pusher.
- the slot defined by the first end portion of the pusher is a first slot, the first end portion of the pusher defining a second slot.
- the slot defined by the first end portion of the pusher is a first slot, the first end portion of the pusher defining a second slot, the first slot extends in a direction parallel to a longitudinal axis of the pusher, the second slot extends is a direction parallel to the longitudinal axis of the pusher.
- the first end portion of the pusher defines a plurality of slots.
- the slot defined by the first end portion of the pusher is a first slot, the first end portion of the pusher defining a second slot, a third slot, and a fourth slot.
- the first end portion of the pusher is configured to be placed in an expanded configuration and a collapsed configuration. In some implementations, the first end portion of the pusher is configured to be placed in an expanded configuration and a collapsed configuration, the first end portion of the pusher being configured to be placed in the collapsed configuration in response to the first end portion of the pusher contacting an inner diameter of the elongate member.
- the first end portion of the pusher includes a first section disposed on a first side of the slot and a second section disposed on a second side of the slot, the first end portion of the pusher is configured to be placed in an expanded configuration and a collapsed configuration, the first section of the pusher being disposed closer to the second section of the pusher when the first end portion of the pusher is disposed in the collapsed configuration than when the first end portion of the pusher is disposed in the expanded configuration.
- the elongate member defines a slot.
- a kit includes a bodily implant; a delivery needle configured to be coupled to the bodily implant: and a delivery device having an elongate member defining a lumen extending from a first end of the elongate member to a second end of the elongate member, and a pusher having a first end portion, the first end portion of the pusher being configured to be disposed within the lumen defined by the elongate member and move from a first position within the lumen defined by the elongate member to a second position within the lumen defined by the elongate member, the first end portion of the pusher defining a slot.
- the elongate member defines a slot configured to receive at least a portion of the delivery needle.
- the slot defined by the first end portion of the pusher extends in a direction parallel to a longitudinal axis of the pusher.
- the slot defined by the first end portion of the pusher is a first slot, the first end portion of the pusher defining a second slot.
- the slot defined by the first end portion of the pusher is a first slot, the first end portion of the pusher defining a second slot, the first slot extends in a direction parallel to a longitudinal axis of the pusher, the second slot extends is a direction parallel to the longitudinal axis of the pusher.
- the first end portion of the pusher defines a plurality of slots.
- FIG. 1 schematically illustrates a system according to an implementation.
- FIG. 2 is a perspective view of an insertion device according to an implementation.
- FIGS. 3 and 4 are cross-sectional views of the insertion device of FIG. 2.
- FIGS. 5 and 6 are cross sectional views of a portion of the insertion device of FIG. 2.
- FIG.7 is a perspective view of an elongate member of the insertion device of FIG. 2.
- FIG. 8 is a cross-sectional view of the elongate member of FIG. 7.
- FIG. 9 is a side view of a coupler of the insertion device of FIG. 2.
- FIG. 10 is a cross-sectional view of the coupler of FIG. 9.
- FIG. 11 is a perspective view of a pusher of the insertion device of
- FIG. 12 is a perspective view of an end portion of the pusher or FIG.
- FIG. 13 is a side view of the insertion device of FIG. 2.
- FIG. 14 is a cross-sectional view of the insertion device taken along line A-A of FIG. 13.
- FIG. 15 is a cross-sectional view of the insertion device taken along line B-B of FIG. 13.
- FIG. 16-18 illustrate a method of using an insertion device according to an implementation.
- the terms “a” or '‘an,” as used herein, are defined as one or more than one.
- the term “another,” as used herein, is defined as at least a second or more.
- the terms “including” and/or “having”, as used herein, are defined as comprising (i.e., open transition).
- the term “coupled” or “moveably coupled,” as used herein, is defined as connected, although not necessarily directly and mechanically.
- the embodiments are directed to medical devices such as insertion devices for penile prostheses or other bodily implants.
- the term patient may hereafter be used for a person who benefits from the medical device or the methods disclosed in the present disclosure.
- the patient can be a person whose body is implanted using the medical device or benefits from the methods disclosed for operating the medical devices of the present disclosure.
- the patient may be a human male, a human female, or any other mammal.
- proximal and distal described in relation to various devices, apparatuses, and components as discussed in the subsequent text of the present disclosure are referred to using a point of reference.
- the point of reference is a perspective of a person who uses the disclosed insertion devices to implant a bodily implant, such as a penile prosthesis.
- the person may be a surgeon, a physician, a nurse, a doctor, a technician, and the like who may perform the implantation procedure.
- proximal refers to an area or portion that is closer or closest to the person during the implantation procedure.
- distal refers to an area or portion that is farther from, or farthest from the person.
- the embodiments discussed herein may provide improvements to penile prosthesis insertion devices (e.g., Furlow insertion devices, Furlow insertion tools, insertion tools, devices, tools, etc.).
- penile prosthesis insertion devices e.g., Furlow insertion devices, Furlow insertion tools, insertion tools, devices, tools, etc.
- such insertion devices can be configured to be used in a single procedure and then discarded or disposed of.
- Some such insertion devices may have components that are coupled together and that when removed from each other would destroy the insertion device.
- FIG. 1 schematically illustrates a system according to an implementation.
- the system includes a delivery or insertion device 100, an implant 195, and a needle 190 coupled to the implant 195.
- the implant 195 may be a penile implant or another type of implant that is configured to be placed in the pelvic region of the patient.
- the implant 195 is configured to be placed within the body of the patient at a different location.
- the needle 190 is coupled to the implant 195 via a suture.
- the needle 190 is directly coupled to the implant 195 or is coupled to the implant 195 via another mechanism.
- the insertion device 100 includes an elongate member 110, a coupler 140, and a pusher or an obturator 170.
- the elongate member 110 is coupled to the coupler 140 and the pusher or obturator 170 is coupled to the coupler 140.
- the elongate member 110 is fixedly coupled to the coupler 140.
- the obturator 170 is moveably, such as slidably, coupled to the coupler 140.
- the pusher or obturator 170 has a portion that is configured to be disposed within a lumen defined by the elongate member 110.
- the needle 190 or a portion of the needle 190 may be placed or disposed within the lumen defined by the elongate member.
- the delivery device 100 including the needle 190 may be placed within the body of the patient to a desired location.
- the pusher or obturator 170 may then be advanced or moved distally within the lumen defined by the elongate member 110.
- the pusher or obturator 170 is configured to engage the needle 190 and advance the needle 190 out of the lumen defined by the elongate member 110.
- the delivery device 100 may then be removed from the body of the patient and the needle can then be pulled or otherwise moved within the body of the patient until the implant 195 is disposed at a desired location.
- FIGS. 2-6 illustrate an insertion device 200 according to an implementation.
- FIG. 2 is a perspective view of the insertion device 200.
- FIGS. 3 and 4 are cross-sectional views of the insertion device.
- FIGS. 5 and 6 are cross sectional views of a portion of the insertion device.
- the insertion device 200 includes an elongate member 210, a coupler 240, and a pusher or obturator 270.
- the elongate member 210 is coupled to the coupler 240 and the pusher or obturator 270 is coupled to the coupler 240.
- the elongate member 210 is fixedly coupled to the coupler 240.
- the coupler 240 defines a lumen 242.
- a proximal end portion 212 of the elongate member 210 is configured to be disposed within the lumen 242 defined by the coupler 240.
- the proximal end portion 212 of the elongate member 210 includes an engagement portion or engagement member 217.
- the engagement portion or member 217 extends from an outer surface 211 of the elongate member 210.
- the coupler 240 also includes an engagement member 244.
- the engagement member 244 of the coupler 240 extends into the lumen 242 defined by the coupler 240.
- the engagement member 244 of the coupler 240 is configured to engage or interact with the elongate member 210 to couple the elongate member 210 to the coupler 240. As best illustrated in FIG. 6, the engagement member 244 of the coupler 240 is configured to engage or interact with the engagement member 217 of the elongate member 210. In some implementations, the engagement member 244 of the coupler 240 is configured to bend or flex to provide a snap type coupling to the elongate member 210. In other implementations, the elongate member 210 is coupled to the coupler via a different mechanism or different ty pe of coupling.
- the pusher or obturator 270 is movably coupled to the coupler 240. At least a portion of the pusher or obturator 270 is disposed within the lumen 242 defined by the coupler 240 and is configured to slide, translate, or otherwise move with respect to the coupler 240.
- the coupler 240 includes an engagement member 246. As will be discussed in more detail below, the engagement member 246 extends into the lumen 242 defined by the coupler 240 and is configured to engage or contact a portion of the pusher or obturator 270.
- At least a portion of the pusher or obturator 270 extends into a lumen 216 defined by the elongate member 210.
- the pusher or obturator 270 is configured to slide or otherwise move within the lumen 216 defined by the elongate member 210.
- a needle that is coupled to a bodily implant may be placed or disposed within the lumen 216 defined by the elongate member 210.
- the delivery device 200 including the needle may be placed within the body of the patient to a desired location.
- the pusher or obturator 270 may then be advanced or moved distally within the lumen 216 defined by the elongate member 210.
- the pusher or obturator 270 is configured to engage the needle and advance the needle out of the lumen 216 defined by the elongate member 210.
- the delivery device 200 may then be removed from the body of the patient and the needle can then be pulled or otherwise moved within the body of the patient until the implant is disposed or located at a desired location.
- FIGS. 7 and 8 illustrate the elongate member 210.
- the elongate member 210 includes or defines a slot 218.
- the slot 218 is disposed at the distal end portion 214 of the elongate member 210 and communicates with the lumen 216 defined by the elongate member 210.
- the slot 218 is configured to receive the needle to facilitate the placement of the needle into the lumen 216 defined by the elongate member 210.
- the elongate member 210 also includes a tapering or tapered portion 213 of the lumen 216 at the distal end portion 214 of the elongate member 210.
- the tapering or narrowing of the lumen 216 helps eject or dispose of the needle more accurately as desired by the user.
- the narrowing or tapering of the lumen 216 of the elongate member 210 may limit the or minimize the exit angle of the needle from the lumen 216.
- the elongate member 210 includes a handle portion 215.
- the handle portion 215 extends from an outer surface 21 1 of the elongate member 210.
- the handle portion 215 may be grasped by the user during the insertion of the delivery' device 200 into the body of the patient and during the advancement or movement of the pusher or obturator 270 with respect to the elongate member 210.
- the elongate member 210 includes measurement markings 219.
- the measurement markings 219 may be configured to indicate to the user how far the elongate member 210 (or the delivery device 200) has been inserted into the body of the patient.
- the measurement markings 219 are laser etched onto the material of the elongate member 210.
- the surface of the elongate member 210 that includes the measurement markings 219 may be smooth.
- the measurement markings 219 may be formed in a different manner.
- the measurement markings 219 may be painted, colored, or otherwise marked on the surface of the elongate member 210.
- FIGS. 9 and 10 illustrate the coupler 240.
- the coupler 240 defines a lumen 242.
- the lumen 242 is configured to receive at least a portion of the elongate member 210 and at least a portion of the obturator 270.
- the coupler includes an engagement member 244 that is configured to engage the elongate member 210 to couple the elongate member 210 to the coupler 240.
- the engagement member 244 extends into the lumen 242 defined by the coupler 240.
- the engagement member 244 is configured to bend or flex.
- the coupler includes an engagement member 246.
- the engagement member 246 extends into the lumen 242 defined by the coupler 240 and is configured to engage the pusher or obturator 270.
- the engagement member 246 is configured to contact or engage the pusher or obturator 270 to help prevent the pusher or obturator 270 from being removed from the coupler 240. Accordingly, the pusher or obturator 270 may move or slide within the lumen 242 defined by the coupler 240 but in some implementations, may not be removed entirely from the lumen 242 of the coupler 240.
- the coupler 240 includes ridges or projections 248 that extend from an outer surface of the coupler 240.
- the ridges or projections 248 may facilitate the grasping or gripping of the coupler 240 or the delivery device 200 during use of the device.
- FIGS. 11 and 12 illustrate the pusher or obturator 270 of the delivery 7 device 200.
- the pusher or obturator 270 includes a distal end portion 276 and a handle portion disposed opposite the distal end portion 276.
- the pusher or obturator 270 includes ramps or bumps 272 A and 272B.
- the ramps or bumps extend from an outer surface 271 of the obturator 270 and are configured to engage the coupler 240.
- the ramps or bumps 272A and 272B are configured to engage the engagement member 246 of the coupler 240.
- the proximal ramps 272A may engage the engagement member 246 of the coupler 240 when the pusher or obturator 270 is placed in its distal most position.
- the distal ramp 272B may be configured to engage the engagement member 246 of the coupler 240 when the obturator is placed in its proximal most position. Additionally, in some implementations, the distal ramps 272B may engage the engagement member 246 of the coupler 240 to help prevent the removal of the pusher or obturator 270 from the coupler 240.
- the pusher or obturator 270 includes an association ramp or bump 274.
- the association ramp or bump 274 is configured to facilitate the association of the pusher or obturator 270 and the coupler 240 and is configured to help prevent the removal of the pusher or obturator 270 from the coupler 240.
- the association ramp or bump 274 is configured to contact or engage the coupler 240 to prevent the removal or disassociation of the pusher or obturator 270 from the coupler 240.
- the distal end 276 of the pusher or obturator 270 defines a series or slots 273.
- the slots 273 extend longitudinally. In other words, the slots 273 extend in a direction parallel to a longitudinal axis LA of the pusher or obturator 270.
- the pusher or obturator 270 defines six slots. In other implementations, the pusher or obturator 270 defines more than six slots.
- the distal end portion 276 may define 8, 10, 12 or more slots. In yet other implementations, the pusher or obturator 270 may define less than six slots.
- the distal end portion 276 may define 1, 2, 3, 4, or 5 slots.
- the slots 273 defined by the distal end portion 276 of the pusher or obturator 270 allow the distal end portion 276 of the pusher or obturator 270 to be placed in an expanded configuration and a collapsed configuration.
- the portions of the pusher or obturator 270 that are disposed adjacent to the slots 273 are configured to flex or bend to allow the outer diameter or other size of the distal end portion to become smaller.
- the pusher or obturator 270 may be moved into its contracted or collapsed configuration.
- portions of the elongate member 210 may have a slightly larger or a slightly smaller inner diameter. These variations may be due to manufacturing processes or due heating and expansion or contraction after the manufacturing process.
- the distal end portion 276 of the pusher or obturator 270 As the distal end portion 276 of the pusher or obturator 270 is configured to expand and collapse, the distal end portion 276 of the pusher or obturator 270 can accommodate small changes in the inner diameter of the elongate member 210. Accordingly, as the pusher or obturator 270 is moved within the lumen defined by the elongate member 210 the pusher or obturator 270 may move smoothly even if the inner diameter of the elongate member 210 varies.
- FIG. 13 is a side view of the insertion device 200.
- FIG. 14 is a cross- sectional view of the insertion device taken along line A-A of FIG. 13.
- FIG. 15 is a cross-sectional view of the insertion device taken along line B-B of FIG. 13.
- the distal end portion 276 of the pusher or obturator 270 can assume an expanded configuration (larger outer diameter and larger spaces between the portions that are adjacent to the slots) when the distal end portion 276 of the pusher or obturator 270 is located at a location of a larger inner diameter of the elongate member 210.
- FIG. 14 is a cross- sectional view of the insertion device taken along line A-A of FIG. 13.
- FIG. 15 is a cross-sectional view of the insertion device taken along line B-B of FIG. 13.
- the distal end portion 276 of the pusher or obturator 270 can assume an expanded configuration (larger outer diameter and larger spaces between the portions that are adjacent to
- the distal end portion 276 of the pusher or obturator 270 can assume a collapsed or compressed configuration (smaller outer diameter and smaller spaces between the portions that are adjacent to the slots) when the distal end portion 276 of the pusher or obturator 270 is located at a location of a smaller inner diameter of the elongate member 210.
- FIGS. 16 to 18 illustrate steps for placing an implant within a body of a patient using a delivery device.
- a needle 290 may be associated with or coupled to an implant 195.
- the needle 290 may be associated with the implant 195 via a suture.
- the needle 290 may be placed within the lumen defined by the elongate member 210 of the delivery device 200.
- the needle 290 may be inserted into the lumen via a slot defined by the elongate member 210.
- the delivery' device 200 may be inserted into the body of the patient, such as into a penis P of the patient.
- the pusher or obturator 270 may then be advanced or moved distally within the lumen defined by the elongate member 210.
- the pusher or obturator 270 is configured to engage the needle 290 and advance the needle 290 out of the lumen defined by the elongate member 210.
- the delivery device 200 may then be removed from the body of the patient and the needle 290 can then be pulled or otherwise moved within the body of the patient until the implant 295 is disposed at a desired location.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Public Health (AREA)
- Cardiology (AREA)
- Reproductive Health (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Vascular Medicine (AREA)
- Transplantation (AREA)
- Surgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pathology (AREA)
- Medical Informatics (AREA)
- Molecular Biology (AREA)
- Prostheses (AREA)
- Media Introduction/Drainage Providing Device (AREA)
- Instruments For Viewing The Inside Of Hollow Bodies (AREA)
Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202480045460.8A CN121487693A (en) | 2023-07-06 | 2024-07-02 | Disposable pheromone insertion device with collapsible pusher |
| AU2024290848A AU2024290848A1 (en) | 2023-07-06 | 2024-07-02 | Disposable furlow insertion device with collapsible pusher |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202363512146P | 2023-07-06 | 2023-07-06 | |
| US63/512,146 | 2023-07-06 | ||
| US18/760,670 | 2024-07-01 | ||
| US18/760,670 US20250009514A1 (en) | 2023-07-06 | 2024-07-01 | Disposable furlow insertion device with collapsible pusher |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2025010282A1 true WO2025010282A1 (en) | 2025-01-09 |
Family
ID=92106624
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2024/036581 Ceased WO2025010282A1 (en) | 2023-07-06 | 2024-07-02 | Disposable furlow insertion device with collapsible pusher |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20250009514A1 (en) |
| CN (1) | CN121487693A (en) |
| AU (1) | AU2024290848A1 (en) |
| WO (1) | WO2025010282A1 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040167574A1 (en) * | 2003-02-26 | 2004-08-26 | Kuyava Charles C. | Keith needle for furlow insertion tool |
| US20100160722A1 (en) * | 2008-12-23 | 2010-06-24 | Ams Research Corporation | Penile prosthesis implantation device |
| US20190290435A1 (en) * | 2018-03-23 | 2019-09-26 | Boston Scientific Scimed, Inc. | Furlow insertion device |
-
2024
- 2024-07-01 US US18/760,670 patent/US20250009514A1/en active Pending
- 2024-07-02 AU AU2024290848A patent/AU2024290848A1/en active Pending
- 2024-07-02 CN CN202480045460.8A patent/CN121487693A/en active Pending
- 2024-07-02 WO PCT/US2024/036581 patent/WO2025010282A1/en not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040167574A1 (en) * | 2003-02-26 | 2004-08-26 | Kuyava Charles C. | Keith needle for furlow insertion tool |
| US20100160722A1 (en) * | 2008-12-23 | 2010-06-24 | Ams Research Corporation | Penile prosthesis implantation device |
| US20190290435A1 (en) * | 2018-03-23 | 2019-09-26 | Boston Scientific Scimed, Inc. | Furlow insertion device |
Also Published As
| Publication number | Publication date |
|---|---|
| CN121487693A (en) | 2026-02-06 |
| US20250009514A1 (en) | 2025-01-09 |
| AU2024290848A1 (en) | 2025-11-27 |
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