CN214017904U - Bone regeneration titanium film for dental implantation - Google Patents

Bone regeneration titanium film for dental implantation Download PDF

Info

Publication number
CN214017904U
CN214017904U CN202023146780.0U CN202023146780U CN214017904U CN 214017904 U CN214017904 U CN 214017904U CN 202023146780 U CN202023146780 U CN 202023146780U CN 214017904 U CN214017904 U CN 214017904U
Authority
CN
China
Prior art keywords
titanium
bone
tooth
titanium film
dentition
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.)
Active
Application number
CN202023146780.0U
Other languages
Chinese (zh)
Inventor
潘留国
江云超
曾敏崧
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shanghai Wujian Medical Instrument Co ltd
Original Assignee
Shanghai Wujian Medical Instrument Co ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shanghai Wujian Medical Instrument Co ltd filed Critical Shanghai Wujian Medical Instrument Co ltd
Priority to CN202023146780.0U priority Critical patent/CN214017904U/en
Application granted granted Critical
Publication of CN214017904U publication Critical patent/CN214017904U/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Prostheses (AREA)
  • Dental Prosthetics (AREA)
  • Materials For Medical Uses (AREA)

Abstract

The utility model discloses a tooth is planted with bone regeneration titanium membrane contains: the titanium film body is used for covering the jaw bone at the position of the tooth to be implanted; the edge of one side of the titanium film body along the dentition direction is provided with a dentition arc-shaped groove or the edges of two sides are respectively provided with a dentition arc-shaped groove, and the shape and the position of the dentition arc-shaped groove are matched with the tooth root of the adjacent tooth of the tooth to be planted; a plurality of blood supply holes penetrating through the titanium membrane body are uniformly distributed on the titanium membrane body; the edge of the titanium film body along the tongue buccal direction is provided with a plurality of titanium film screw fixing holes. The utility model discloses can cover in the alveolar bone cheek in lack tooth area, tongue side position, can prune according to how much needs of bone volume, easily mould the type, easily fix, can also avoid the infection and the wound fracture that cause with the root of a tooth contact, damage mental nerve when avoiding planting the operation, can satisfy tooth and plant required bone volume and promote the use, effectively improve tooth and plant the success rate that guides bone regeneration art.

Description

Bone regeneration titanium film for dental implantation
Technical Field
The utility model relates to the technical field of dental medical equipment, in particular to a bone regeneration titanium film for dental implantation.
Background
Dental implantation is one of the important surgical methods of the current dental restoration, and the main reason for the failure of dental implantation is that the bone mass of the jaw bone of a patient is insufficient, so that the implanted dental implant is loosened and fails. The proper horizontal and vertical direction of patient's jaw promotes patient's bone volume, increases dental implant's firmness, is the most crucial factor of preventing dental implantation failure.
The bone induction regeneration technology is clinically introduced into the field of dental implantation, and the principle of the technology is that a bone regeneration film is pasted on a part needing bone mass lifting to form a certain cavity, and artificial bone powder or autologous bone fragments are filled to induce the artificial bone powder to form bone. Whether the bone regeneration membrane can provide a stable cavity and cannot expose infection is a key factor influencing the osteogenesis effect.
Currently, the guided bone regeneration membranes commonly used in clinic are divided into two major types, i.e., absorbable membranes and non-absorbable membranes. The absorbable guide bone regeneration membrane is mostly designed into a double-layer membrane form, such as a Bio-Gide collagen membrane which is a product on the market and a tissue regeneration membrane provided by a patent CN 104474589A, wherein one layer is a compact layer and plays a role of a cell barrier and prevents soft tissue cells from growing into a bone defect area; the other layer is a loose layer which can induce new cells to grow into the loose layer and can be used as a support for cell growth to promote bone tissue regeneration. However, for the dental implant bone lifting operation, artificial bone powder is often required to be filled to induce bone tissue regeneration, the support property of an absorbable membrane is insufficient, the absorbable membrane is easy to collapse, a stable cavity cannot be formed, and the absorbable membrane cannot play a supporting role; in addition, once the absorbable membrane is degraded too early, the absorbable membrane cannot play a biological barrier role, muscle fibrous tissues grow into the artificial bone powder, so that cancellous bone is easily formed, compact cortical bone tissues cannot be formed, and the implant loosening failure is caused; absorbable membranes also have surgical risks of being unable to fix, causing displacement of the membrane, and the like.
Non-absorbable bone regeneration membranes, such as e-PTFE (expanded polytetrafluoroethylene, Expamded PTFE, e-PTFE) membranes, are also not sufficiently supportive and tend to collapse; the e-PTFE membrane limits the growth of soft tissues to a bone defect area, simultaneously limits the blood supply and protection of the soft tissues to a wound area, is often accompanied by the risks of slow healing of postoperative wounds and even cracking, and the risks of exposure of a regeneration membrane and postoperative infection caused by the cracking of the wounds are also accompanied.
The titanium membrane can effectually provide the support nature, but, the titanium membrane that uses clinically, thickness is thicker, is difficult to prune, is difficult to cause the wound to sew up the difficulty according to the form shaping of patient's jaw easily, leads to wound fracture, titanium membrane to expose etc. and leads to bone to promote the operation failure. Patent CN 106937896 a provides a titanium metal mesh, which is formed by pressing and designing fine titanium wires, but the technical process is complex, a large number of specifications and models need to be prefabricated, and the barrier function of the metal mesh needs to be further verified.
Disclosure of Invention
According to the embodiment of the utility model provides a bone regeneration titanium membrane for dental implantation contains:
the titanium film body is used for covering the jaw bone at the position of the tooth to be implanted;
the edge of one side of the titanium film body along the dentition direction is provided with a dentition arc-shaped groove or the edges of two sides are respectively provided with a dentition arc-shaped groove, and the shape and the position of the dentition arc-shaped groove are matched with the tooth root of the adjacent tooth of the tooth to be planted;
a plurality of blood supply holes penetrating through the titanium membrane body are uniformly distributed on the titanium membrane body;
the edge of the titanium film body along the tongue buccal direction is provided with a plurality of titanium film screw fixing holes.
Furthermore, the thickness range of the titanium film body is 0.05-0.15 mm.
Furthermore, the titanium film body is also provided with a plurality of dental implant mounting holes which are distributed along the dentition direction.
Furthermore, the number of the mounting holes of the dental implant ranges from 1 to 3.
Furthermore, the diameter range of the dental implant mounting holes is 2.0-5.0 mm, and the distance range of the adjacent dental implant mounting holes is 6-15 mm.
Further, a mental foramen groove is arranged on the edge of one side of the titanium membrane body along the direction of the cheek side, and after the titanium membrane body is installed on the jaw bone, the mental foramen groove corresponds to the mental foramen on the jaw bone.
Furthermore, the mental foramen slot is U-shaped.
Furthermore, the diameter range of the blood supply hole is 0.2-1.0 mm.
Furthermore, the diameter range of the titanium film screw fixing hole is 0.6-1.6 mm.
Furthermore, the edge of the titanium film body along the dentition direction is in a sawtooth shape.
According to the utility model discloses dental implantation is with bone regeneration titanium membrane can cover in the alveolar bone cheek in lack tooth area, tongue side position, can prune according to how much needs of bone mass, easily mould the type, easily fixed, can also avoid the infection and the wound fracture that cause with the root of a tooth contact, damage mental nerve when avoiding planting the operation, can satisfy the tooth and plant required bone mass and promote the use, effectively improve the success rate that the tooth planted and guide bone regeneration art.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and are intended to provide further explanation of the claimed technology.
Drawings
FIG. 1 is a schematic structural view of a dental implant installation hole of a bone regeneration titanium film for dental implantation according to an embodiment of the present invention;
FIG. 2 is a schematic structural view of a dental implant mounting hole of a bone regeneration titanium film for dental implantation according to an embodiment of the present invention;
FIG. 3 is a schematic view of the installation principle of FIG. 2;
FIG. 4 is a schematic structural view of a dental implant bone regeneration titanium membrane without a mental foramen groove according to an embodiment of the present invention;
FIG. 5 is a schematic structural view of a dental implant made of a bone regeneration titanium film for dental implant according to an embodiment of the present invention, which is used for dental implant for elevating bone mass only at a buccal side and forming a mental foramen;
fig. 6 is a schematic structural view of a dental implant made of a bone regeneration titanium membrane according to an embodiment of the present invention, which is used for dental implant for elevating bone mass only at a buccal side position and not forming a mental foramen groove.
Detailed Description
The present invention will be further described with reference to the following detailed description of preferred embodiments thereof, which is to be read in connection with the accompanying drawings.
First, a bone regeneration titanium membrane for dental implantation according to an embodiment of the present invention will be described with reference to fig. 1 to 6, which is used for dental implantation and has a wide application range.
As shown in figures 1-3, the utility model discloses tooth is planted and is used bone regeneration titanium membrane has titanium membrane body 1, and titanium membrane body 1 is used for covering on jaw 2 of the tooth position of waiting to plant. In this embodiment, the thickness of the titanium film body 1 is in the range of 0.05 to 0.15 mm.
Specifically, as shown in fig. 1-2, a dentition arc-shaped groove 11 is formed in the edge of one side of the titanium film body 1 along the dentition direction a-a, or a dentition arc-shaped groove 11 is formed in the edge of each of two sides of the titanium film body 1, the shape and the position of each dentition arc-shaped groove 11 are matched with the tooth root 4 of an adjacent tooth of a tooth to be planted, when the titanium film body is installed, a gap of 2-5 mm is formed between the edge of each dentition arc-shaped groove 11 and the outer edge of the tooth root 4, the titanium film is prevented from contacting with the tooth root 4, and the titanium film is prevented from being exposed due to contact of saliva, food residues and the like with the titanium film, so that postoperative infection and wound cracking are caused.
Specifically, as shown in fig. 1 to 6, a plurality of blood supply holes 12 penetrating through the titanium membrane body 1 are uniformly distributed on the titanium membrane body 1, and in this embodiment, the diameter range of the blood supply holes 12 is 0.2 to 1.0mm, which not only can effectively provide blood supply, but also can prevent soft tissue from growing into the artificial bone powder.
Specifically, as shown in fig. 1 to 6, a plurality of titanium film screw fixing holes 13 are formed in the edge of the titanium film body 1 along the tongue-and-cheek direction B-B to prevent the titanium film body 1 from warping and shifting, in this embodiment, the diameter range of the titanium film screw fixing holes 13 is 0.6 to 1.6 mm.
Specifically, as shown in fig. 2 to 6, the titanium film body 1 is further provided with a plurality of dental implant mounting holes 14, the plurality of dental implant mounting holes 14 are distributed along the dentition direction a-a, in this embodiment, the number of the dental implant mounting holes 14 is 1 to 3, the diameter range of the dental implant mounting holes 14 is 2.0 to 5.0mm, and the distance range between adjacent dental implant mounting holes 14 is 6 to 15 mm.
Further, as shown in fig. 4 and 6, when it is installed, the titanium film body 1 directly buried under the gum tissue is not provided with the dental implant installation hole 14, and can be extended in a saddle shape such as shown in fig. 4, and can be extended in a saw-toothed structure when it is only necessary to raise the bone quantity at the buccal position, and can be trimmed to a one-sided saw-toothed structure as shown in fig. 5 and 6 as needed.
Specifically, as shown in fig. 1 to 3 and 5, a mental nerve hole groove 15 is formed in an edge of one side of the titanium membrane body 1 in the tongue-and-cheek direction B-B, and after the titanium membrane body 1 is mounted on the jaw bone 2, the mental nerve hole groove 15 corresponds to the mental nerve hole 3 in the jaw bone 2, so that the mental nerve is prevented from being damaged. In this embodiment, the mental foramen 3 slot 15 is U-shaped, completely covering the mental foramen 3.
Further, as shown in fig. 4 and 6, when the position other than the mental foramen needs to lift the bone mass, the mental foramen 3 groove 15 does not need to be opened.
Further, when the bone mass is required to be lifted only at the buccal position, the zigzag structure shown in fig. 5 and 6 can be extended, that is, the edge of the titanium film body 1 along the dentition direction a-a is zigzag, so that the bending formation during the installation of the titanium film body 1 is facilitated.
When the device is installed, the titanium film body 1 is covered on the buccal and lingual sides of the alveolar bone of the edentulous area, the proper titanium film body 1 is selected according to the bone mass and position, and the titanium film body 1 is trimmed, shaped and fixed.
Above, having described with reference to fig. 1~6 and having used the bone regeneration titanium membrane according to the utility model discloses dental implantation can cover in the alveolar bone cheek that lacks the tooth district, tongue side position, can prune according to how much needs of bone mass, easily mould the type, easily fix, can also avoid infection and the wound fracture that leads to the fact with the root of a tooth contact, damage mental nerve when avoiding planting the operation, can satisfy the required bone mass promotion of dental implantation and use, effectively improve the success rate of dental implantation guide bone regeneration.
It should be noted that, in the present specification, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising … …" does not exclude the presence of other identical elements in a process, method, article, or apparatus that comprises the element.
While the present invention has been described in detail with reference to the preferred embodiments thereof, it should be understood that the above description should not be taken as limiting the present invention. Numerous modifications and alterations to the present invention will become apparent to those skilled in the art upon reading the foregoing description. Accordingly, the scope of the invention should be limited only by the attached claims.

Claims (10)

1. A bone regeneration titanium membrane for dental implantation, comprising:
the titanium film body is used for covering the jaw bone at the position of the tooth to be implanted;
the titanium film body is provided with a dentition arc-shaped groove along one side edge of the dentition direction or two side edges of the dentition arc-shaped groove respectively, and the shape and the position of the dentition arc-shaped groove are matched with tooth roots of adjacent teeth of the teeth to be planted;
a plurality of blood supply holes penetrating through the titanium membrane body are uniformly distributed on the titanium membrane body;
and a plurality of titanium film screw fixing holes are formed in the edge of the titanium film body along the tongue buccal direction.
2. The dental implant bone regeneration titanium membrane according to claim 1, wherein the thickness of the titanium membrane body is in a range of 0.05 to 0.15 mm.
3. The dental bone regeneration titanium mask for implantation as claimed in claim 1 or 2, wherein the titanium mask body further comprises a plurality of dental implant mounting holes, and the plurality of dental implant mounting holes are distributed along the dentition direction.
4. The titanium film for regenerating bone for dental implantation according to claim 3, wherein the number of the dental implant mounting holes is in the range of 1 to 3.
5. The titanium film for regenerating bone for dental implantation as claimed in claim 3, wherein the diameter of said dental implant mounting hole is in the range of 2.0 to 5.0mm, and the distance between adjacent ones of said dental implant mounting holes is in the range of 6 to 15 mm.
6. The dental implant bone regeneration titanium membrane according to claim 1 or 2, wherein a mental foramen groove is provided on one side edge of the titanium membrane body in the buccal direction, and after the titanium membrane body is mounted on a jaw bone, the mental foramen groove corresponds to the mental foramen on the jaw bone.
7. The dental implant bone regeneration titanium membrane of claim 6, wherein the mental foramen trough is U-shaped.
8. The titanium film for regenerating bone for dental implantation as claimed in claim 1 or 2, wherein the diameter of said blood supply hole is in the range of 0.2 to 1.0 mm.
9. The dental implant bone regeneration titanium membrane according to claim 1 or 2, wherein the diameter of the screw fixation hole of the titanium membrane is in the range of 0.6 to 1.6 mm.
10. The dental bone regeneration titanium membrane for implantation according to claim 1 or 2, wherein an edge of the titanium membrane body in the dentition direction is serrated.
CN202023146780.0U 2020-12-24 2020-12-24 Bone regeneration titanium film for dental implantation Active CN214017904U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202023146780.0U CN214017904U (en) 2020-12-24 2020-12-24 Bone regeneration titanium film for dental implantation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202023146780.0U CN214017904U (en) 2020-12-24 2020-12-24 Bone regeneration titanium film for dental implantation

Publications (1)

Publication Number Publication Date
CN214017904U true CN214017904U (en) 2021-08-24

Family

ID=77341883

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202023146780.0U Active CN214017904U (en) 2020-12-24 2020-12-24 Bone regeneration titanium film for dental implantation

Country Status (1)

Country Link
CN (1) CN214017904U (en)

Similar Documents

Publication Publication Date Title
Nemcovsky et al. Rotated split palatal flap for soft tissue primary coverage over extraction sites with immediate implant placement. Description of the surgical procedure and clinical results
US5700479A (en) Surgical element and method for selective tissue regeneration
CA1246905A (en) Dental implant with expanded ptfe gingival interface
US5093179A (en) Methods and articles for treating periodontal disease and bone defects
JPS6024836A (en) Mouth implant for specially large opening of tooth support
CN203458482U (en) Membrane screw system for guiding regeneration of alveolar bone
CN107260340A (en) The protection structure of Alveolar Bone Defect bone graft area
Williams et al. Immediate teeth in fibulas: expanded clinical applications and surgical technique
JPH0519420B2 (en)
CN214549665U (en) Bone regeneration e-PTFE-Ti composite membrane for dental implantation
CN106073917B (en) Dental implant gum transplants resting guide, guide plate production method and fixed system
EP0773750A1 (en) Surgical element and method for selective tissue regeneration
CN208193177U (en) The protection structure of Alveolar Bone Defect bone graft area
US5607689A (en) Latex element designed to achieve guided tissue regeneration in periodontal dental therapy
CN214017904U (en) Bone regeneration titanium film for dental implantation
CN210811770U (en) Absorbable plastic barrier for implants
Kahnberg et al. Maxillary osteotomy with an interpositional bone graft and implants for reconstruction of the severely resorbed maxilla: a clinical report.
Bruschi et al. Alveolar augmentation: new application for implants
CN1562388A (en) Patch of oral cavity tissue and preparation method and application
CN103494649A (en) Improvement of bone splitting carried out below lip-cheek crest in oral implantation
RU2551936C1 (en) Dental implant
JPH0638807B2 (en) Implant set
WO2013039076A1 (en) Bone augmentation tool
CN210472306U (en) Plant healing base station
CN215130544U (en) Dental implant

Legal Events

Date Code Title Description
GR01 Patent grant
GR01 Patent grant