WO2017002223A1 - Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe - Google Patents

Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe Download PDF

Info

Publication number
WO2017002223A1
WO2017002223A1 PCT/JP2015/068950 JP2015068950W WO2017002223A1 WO 2017002223 A1 WO2017002223 A1 WO 2017002223A1 JP 2015068950 W JP2015068950 W JP 2015068950W WO 2017002223 A1 WO2017002223 A1 WO 2017002223A1
Authority
WO
WIPO (PCT)
Prior art keywords
bone
implant
sliding contact
contact portion
joint
Prior art date
Application number
PCT/JP2015/068950
Other languages
English (en)
Japanese (ja)
Inventor
石渡暉夫
Original Assignee
株式会社ナントー
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 株式会社ナントー filed Critical 株式会社ナントー
Priority to JP2016501909A priority Critical patent/JPWO2017002223A1/ja
Priority to PCT/JP2015/068950 priority patent/WO2017002223A1/fr
Publication of WO2017002223A1 publication Critical patent/WO2017002223A1/fr

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C8/00—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools
    • 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
    • A61F2/30—Joints

Definitions

  • the present invention relates to an implant, a fixture, an abutment, a proximal bone component, and a distal bone component.
  • the present invention relates to a dental implant embedded in a jaw bone and an artificial joint implant embedded in a hip joint or the like.
  • Implants that are implanted in the body are drawing attention.
  • a dental implant is inserted into a hole provided in an alveolar bone and fixed when the root of a permanent tooth is lost due to decay or damage.
  • This dental implant is composed of a fixture (artificial tooth root) fixed to the alveolar bone and an abutment (abutment) screwed to the fixture.
  • An implant crown (artificial dental crown) is attached to the abutment.
  • Dental implants (fixtures, abutments) are made of ceramics such as alumina and zirconia, in addition to metals such as titanium and titanium alloys.
  • the fixture has a hole that opens at the tip surface.
  • a tapered hole is formed in this hole.
  • the abutment is formed with a tapered shaft portion that is inserted into the tapered hole portion.
  • the tapered hole portion and the tapered shaft portion serve as a pressure-resistant portion that receives the occlusal pressure.
  • a pressure-resistant portion tapeer hole portion, taper shaft portion
  • the tapered hole portion and the tapered shaft portion are in close contact (contact) and repeatedly receive the occlusal pressure.
  • fine wear powder is generated from the pressure resistant part.
  • contact between the tapered hole portion and the tapered shaft portion is hindered, and stress concentration occurs in a part of the pressure resistant portion.
  • Ceramics are brittle materials and do not plastically deform like metals. For this reason, when stress concentration occurs in a part of the pressure-resistant portion, a crack occurs in the pressure-resistant portion. In the worst case, the crack progresses and the fixture and abutment are damaged.
  • Artificial joint implants may also be formed of ceramics such as alumina and zirconia.
  • proximal bone component and the distal bone component are made of ceramics, wear powder is generated by sliding the distal bone component against the proximal bone component. For this reason, as with a dental implant, the proximal bone component and the distal bone component are cracked and damaged. In addition, if the wear powder continues to be released from the artificial joint implant, there is a possibility of adversely affecting the human body.
  • An object of the present invention is to provide an implant, a fixture, an abutment, a proximal bone component, and a distal bone component capable of preventing cracks and breakage over a long period of time in ceramic dental implants and artificial joints. Is to provide.
  • a first embodiment of an implant according to the present invention includes a ceramic implant body fixed to a bone, and a ceramic connection body having a contact portion that comes into contact with a contacted portion formed on the implant body, A sealing body that is disposed between the contacted portion and the contact portion, and seals wear powder generated from the contacted portion and the contact portion; It is characterized by providing.
  • the second embodiment of the implant according to the present invention is characterized in that, in the first embodiment, the sealing body prevents the generation of the abrasion powder.
  • the third embodiment of the implant according to the present invention is characterized in that, in the first or second embodiment, the sealing body is arranged in a region not touching the bone.
  • the sealing body is fixed to the contacted part and / or the contact part. It is characterized by.
  • the fifth embodiment of the implant according to the present invention is characterized in that in the fourth embodiment, the implant has radiation resistance and heat resistance.
  • the sixth embodiment of the implant according to the present invention is characterized in that, in any one of the first to fifth embodiments, the sealing body is made of a polymer of paraxylylene.
  • the seventh embodiment of the implant according to the present invention is characterized in that, in any one of the first to sixth embodiments, the sealing body has a thickness of 0.1 ⁇ m or more and 50 ⁇ m or less.
  • An eighth embodiment of the implant according to the present invention is the implant according to any one of the first to seventh embodiments, wherein the implant body is a fixture embedded in an alveolar bone, and the connection body is fitted to the fixture. It is an abutment that performs.
  • the contacted portion is a tapered hole portion whose diameter is reduced in the depth direction, and the contact portion is reduced toward the proximal end side.
  • a tenth embodiment of the implant according to the present invention is the implant according to any one of the first to seventh embodiments, wherein the implant body is a proximal bone component fixed to a bone on a proximal side of a joint, and the connection The body is a distal bone component that is fixed to the bone on the distal end side of the joint and is in sliding contact with the proximal bone component.
  • the contacted portion is a cup recessed in a spherical shape or an arc shape, and the contact portion protrudes in a spherical shape or an arc shape.
  • a head wherein the cup and the head are in sliding contact with each other through the sealing body.
  • the twelfth embodiment of the implant according to the present invention is characterized in that, in the eleventh embodiment, the joint is a hip joint, a shoulder joint or an ankle.
  • the contacted portion is a head protruding in a spherical shape or an arc shape, and the contact portion is recessed in a spherical shape or an arc shape. It is a cup, The said head and the said cup are slidably contacted via the said sealing body, It is characterized by the above-mentioned.
  • the fourteenth embodiment of the implant according to the present invention is characterized in that, in the thirteenth embodiment, the joint is a knee joint, a shoulder joint or an elbow joint.
  • a first embodiment of a fixture according to the present invention is a ceramic fixture fixed to an alveolar bone, and has a fitted portion to which a fitting portion formed on a metal abutment is fitted.
  • produced from the said to-be-fitted part is arrange
  • a second embodiment of the fixture according to the present invention is a metal fixture fixed to the alveolar bone, and has a fitted portion to which a fitting portion formed on a ceramic abutment is fitted.
  • produced from the said fitting part is arrange
  • a first embodiment of an abutment according to the present invention is a ceramic abutment that is fitted to a metal fixture that is fixed to an alveolar bone, and is fitted into a fitting portion formed in the fixture.
  • combine and seals the abrasion powder generated from the said fitting part is arrange
  • a second embodiment of the abutment according to the present invention is a metal abutment that fits into a ceramic fixture that is fixed to the alveolar bone, and is fitted into a fitting portion formed in the fixture.
  • a sealing body that has a mating portion to be joined and seals abrasion powder generated from the mated portion is disposed in the fitting portion.
  • a first embodiment of a proximal bone component according to the present invention is a ceramic proximal bone component fixed to a bone on the proximal side of a joint, and is fixed to the bone on the distal side of the joint.
  • the sliding contact portion formed on the metal distal bone component has a sliding contact portion, and a sealing body for sealing the abrasion powder generated from the sliding contact portion is disposed in the sliding contact portion. It is characterized by being.
  • a second embodiment of the proximal bone component according to the present invention is a metallic proximal bone component that is fixed to the bone on the proximal side of the joint, and is fixed to the bone on the distal side of the joint.
  • a sliding contact portion formed on the distal end bone component made of ceramics has a sliding contact portion that is in sliding contact, and a sealing body that seals wear powder generated from the sliding contact portion is disposed in the sliding contact portion. It is characterized by that.
  • a first embodiment of the distal bone component according to the present invention is a ceramic distal bone component that is fixed to the bone on the distal end side of the joint, and is made of metal that is fixed to the bone on the proximal end side of the joint.
  • a sealing body that has a sliding contact portion that is in sliding contact with a sliding contact portion formed on the proximal bone component of the sealing member and that seals abrasion powder generated from the sliding contact portion is disposed in the sliding contact portion. It is characterized by.
  • a second embodiment of the distal bone component according to the present invention is a metal distal bone component that is fixed to the bone on the distal end side of the joint, and is made of ceramics that is fixed to the bone on the proximal end side of the joint.
  • a sealing body that has a sliding contact portion that is in sliding contact with the sliding contact portion formed on the proximal bone component of the sealing member and seals abrasion powder generated from the sliding contact portion is disposed in the sliding contact portion. It is characterized by that.
  • the implant, fixture, abutment, proximal bone component, and distal bone component according to the present invention seal ceramic wear powder. This prevents cracking and breakage in ceramics over a long period of time.
  • FIG. 2 is an exploded perspective view of a dental implant 5.
  • FIG. 2 is a side view of a dental implant 5.
  • FIG. It is a figure which shows the dental implant 5, Comprising: (a) Top view, (b) Longitudinal section (IV-IV section).
  • FIG. 5 is a cross-sectional view of the dental implant 5 including (a) Va-Va cross section, (b) Vb-Vb cross section, (c) Vc-Vc cross section, (d) Vd-Vd cross section, (e) Ve-Ve. Section, (f) Vf-Vf section.
  • 1 is a longitudinal sectional view showing a fixture 10.
  • FIG. 8 shows the abutment unit 8, Comprising: (a) Top view, (b) Side surface and longitudinal cross-sectional view (VIIb-VIIb cross section), (c) Bottom view.
  • FIG. 20 Comprising: It is (a) side view, (b) longitudinal cross-sectional view (VIIIb-VIIIb cross section), (c) bottom view.
  • FIG. 30 shows the clamper pin 30, Comprising: (a) Side view, (b) It is a bottom view.
  • 4A and 4B are diagrams showing the clamper 40, where FIG. 4A is a side view, FIG. 4B is a bottom view, and FIG. 4C is a longitudinal sectional view (Xc-Xc cross section).
  • FIG. 4A and 4B are diagrams showing a lock nut 50, where FIG. 5A is a top view, and FIG. 5B is a longitudinal sectional view (XIb-XIb cross section). It is a figure which shows the result of the fatigue test (comparison test) of the dental implant 5. FIG. It is a figure which shows the result of the fatigue test (endurance test) of the dental implant 5.
  • FIG. It is a figure showing artificial hip joint implant 105 concerning an embodiment of the present invention. It is a figure which shows the artificial knee joint implant 115 which concerns on embodiment of this invention. It is a figure which shows the artificial shoulder joint implant 125 which concerns on embodiment of this invention. It is a figure which shows the inversion type shoulder prosthesis joint implant 135 which concerns on embodiment of this invention. It is a figure which shows the artificial elbow joint implant 145 which concerns on embodiment of this invention. It is a figure which shows the artificial ankle implant 155 which concerns on embodiment of this invention.
  • FIG. 1 is a diagram showing a dental implant 5 according to an embodiment of the present invention.
  • the dental implant (implant) 5 includes a fixture 10 fixed to the alveolar bone (bone) 2 and an abutment unit 8 fitted to the fixture 10.
  • An abutment unit 8 is fitted with an implant crown 6.
  • the proximal end side of the implant crown 6 is covered with the gum 4.
  • the longitudinal direction of the dental implant 5 is referred to as the Z direction, the axial direction, or the longitudinal direction.
  • the fixture 10 side is referred to as + Z direction, + Z side, proximal side, or depth direction.
  • the end in the + Z direction is called the base end.
  • the implant crown 6 side is referred to as the ⁇ Z direction, the ⁇ Z side, or the distal end side.
  • the end in the ⁇ Z direction is called the tip.
  • the direction orthogonal to the Z direction is referred to as horizontal.
  • the bottom view is when viewed from the + Z direction, and the top view is when viewed from the -Z direction.
  • a male screw 12 is formed on the outer peripheral surface of the fixture 10.
  • the fixture 10 is fixed to the alveolar bone 2 by screwing a male screw 12 into a hole formed in the alveolar bone 2.
  • An implant crown 6 is mounted on the outer peripheral surface of the abutment unit 8 on the distal end side ( ⁇ Z direction) using an adhesive or the like.
  • FIG. 2 is an exploded perspective view of the dental implant 5 of the present embodiment.
  • FIG. 3 is a side view of the dental implant 5.
  • 4A and 4B are views showing the dental implant 5, wherein FIG. 4A is a top view and FIG. 4B is a longitudinal sectional view (IV-IV section).
  • FIG. 5 is a cross-sectional view of the dental implant 5, wherein (a) Va-Va cross section, (b) Vb-Vb cross section, (c) Vc-Vc cross section, (d) Vd-Vd cross section, (e ) Ve-Ve cross section, (f) Vf-Vf cross section.
  • FIG. 6 is a longitudinal sectional view showing the abutment unit 8.
  • the dental implant 5 includes a fixture 10 and an abutment unit 8.
  • the abutment unit 8 is an assembly of the abutment 20, the clamper pin 30, the clamper 40, and the lock nut 50. Further, the dental implant 5 includes a sealing film 9 disposed between the fixture 10 and the abutment unit 8 (abutment 20).
  • FIGS. 7A and 7B are views showing the fixture 10, wherein (a) a top view, (b) a side surface and a longitudinal sectional view (VIIb-VIIb cross section), and (c) a bottom view.
  • the fixture 10 is a cylindrical member and is formed of a ceramic material such as zirconia.
  • a male screw 12 is provided on the outer peripheral surface of the fixture (implant body) 10.
  • a center hole 13 is opened at the center of the end face on the ⁇ Z side of the fixture 10.
  • a tapered hole portion 14, a reverse tapered hole portion 15, and an engagement hole portion 16 are continuously formed in the depth direction (+ Z direction).
  • the inner diameter of the tapered hole portion (contacted portion, fitted portion) 14 is gradually reduced (reduced) toward the + Z direction.
  • the reverse taper hole 15 gradually increases in diameter (expands) in the + Z direction.
  • the engaging hole portion 16 is formed with two parallel surfaces 16A composed of two parallel inner surfaces facing each other.
  • the taper angle of the taper hole 14 is, for example, 4 °.
  • the length (depth) of the tapered hole portion 14 is formed to be 1/3 or more (for example, 4 to 5 mm) of the entire length (for example, 10 mm) of the fixture 10.
  • the length of the tapered hole portion 14 is formed to be about 3/5 (for example, 8 mm) of the entire length (for example, 12 mm) of the fixture 10.
  • a plurality of protrusions 17 are formed along the Z direction on the inner peripheral side surface of the tapered hole portion 14.
  • the plurality of protrusions 17 are arranged at equal intervals (equal angles) in the circumferential direction of the center hole 13. There are five protrusions 17.
  • the shape of the cross section of the protrusion 17 is a shape that swells into a semicircular arc.
  • a small diameter portion 15A, a reverse taper portion 15B, and a large diameter portion 15C are continuously formed in the reverse tapered hole portion 15 in the + Z direction.
  • the inner diameter of the small diameter portion 15 ⁇ / b> A is smaller than the minimum inner diameter of the tapered hole portion 14.
  • the reverse taper portion 15B has an inner diameter that gradually increases (expands) in the + Z direction.
  • the taper angle of the reverse taper portion 15B is, for example, 10 °.
  • the length (depth) of the reverse tapered portion 15B is, for example, 0.25 mm.
  • the inner diameter of the large diameter portion 15C is larger than the inner diameter of the small diameter portion 15A.
  • the length (depth) of the large diameter portion 15C is, for example, 1.0 mm. Accordingly, the small diameter portion 15 ⁇ / b> A of the reverse tapered hole portion 15 protrudes toward the inner peripheral side of the center hole 13.
  • the engaging hole portion 16 includes two opposing arc-shaped inner peripheral side surfaces and two parallel and opposing inner side surfaces (parallel two surfaces 16A).
  • the length (depth) of the engagement hole 16 is, for example, 0.8 mm.
  • the width (two-surface width) of the two parallel two surfaces 16A is about 0.7 mm.
  • FIGS. 8A and 8B are diagrams showing the abutment 20, wherein FIG. 8A is a side view, FIG. 8B is a vertical cross-sectional view (cross section VIIIb-VIIIb), and FIG. 8C is a bottom view.
  • the abutment (connector) 20 is a shaft-shaped member, and is formed of a white ceramic material having excellent aesthetics. For example, zirconia is used as the ceramic material.
  • the abutment 20 is fitted in the center hole 13 of the fixture 10 on the proximal end side, and the implant crown 6 is mounted on the distal end side.
  • the abutment 20 includes a main body portion 21 and a tapered shaft portion 22.
  • the implant crown 6 is attached to the main body 21.
  • the tapered shaft portion 22 extends from the base end side (+ Z side) of the main body portion 21 and is inserted into the center hole 13 of the fixture 10.
  • the taper angle of the taper shaft portion (contact portion, fitting portion) 22 is, for example, 4 °. That is, it is the same as the angle of the tapered hole portion 14 of the center hole 13 of the fixture 10.
  • the length of the tapered shaft portion 22 is the same as or longer than that of the tapered hole portion 14.
  • the length of the taper shaft portion 22 is, for example, 8.1 mm.
  • a plurality of groove portions 23 are formed on the outer peripheral side surface of the tapered shaft portion 22 along the Z direction.
  • the plurality of groove portions 23 are arranged at equal intervals (equal angles) in the circumferential direction of the tapered shaft portion 22.
  • the shape of the cross section of the groove part 23 is a shape recessed in a semicircular arc shape. That is, the shape is the opposite of the protrusion 17 formed on the inner peripheral side surface of the tapered hole portion 14.
  • the tapered shaft portion 22 of the abutment 20 When the tapered shaft portion 22 of the abutment 20 is inserted into the center hole 13 of the fixture 10, the tapered shaft portion 22 is fitted into the tapered hole portion 14 of the center hole 13.
  • an external force occlusion pressure F
  • the tapered hole portion 14 and the tapered shaft portion 22 function as the pressure-resistant portion 60 (see FIGS. 5C and 5D).
  • the five groove portions 23 are inserted into the five protrusions 17 and are brought into close contact with each other. Since the five protrusions 17 and the five groove portions 23 mesh with each other, the rotation of the abutment 20 relative to the fixture 10 can be suppressed. That is, the protrusion 17 and the groove portion 23 function as the rotation preventing portion 70 (see FIGS. 5C and 5D).
  • a through hole 24 penetrating in the Z direction is formed at the center of the abutment 20.
  • a portion corresponding to the main body portion 21 (main body portion side through hole 24 ⁇ / b> A) has an inner diameter of about 2.5 mm.
  • a lock nut 50 is inserted into the main body side through hole 24A.
  • a portion corresponding to the tapered shaft portion 22 (taper shaft portion side through hole 24 ⁇ / b> B) has an inner diameter of about 1 mm.
  • the main body portion 31 of the clamper pin 30 is inserted through the tapered shaft portion side through hole 24B with almost no gap.
  • a step surface 25 facing the ⁇ Z direction is formed at the boundary between the main body side through hole 24A and the tapered shaft side through hole 24B.
  • the sealing film (sealing body) 9 is disposed (fixed) on the tapered shaft portion 22 of the abutment 20.
  • the sealing film 9 is a solid that generates shear stress in a stationary state. That is, the sealing film 9 is different from a movable object such as a fluid or liquid. Specifically, the sealing film 9 is an object different from a caulking agent or an adhesive.
  • the sealing film 9 is, for example, a resin film.
  • the sealing film 9 is made of, for example, a paraxylylene polymer.
  • the paraxylylene polymer is colorless and transparent.
  • As the polymer of paraxylylene for example, diX (registered trademark) of Sansei Kasei Co., Ltd. or Parylene (registered trademark) of Japan Parylene LLC can be used.
  • the paraxylylene polymer is a resin that is safe to the human body and has high wear resistance, chemical resistance, insulation, and moisture resistance. For this reason, the polymer of paraxylylene is suitable as a material to be disposed in the dental implant 5.
  • the sealing film 9 is coated on the tapered shaft portion 22 of the abutment 20.
  • the sealing film 9 is coated (deposited) by chemical vapor deposition (CVD).
  • the sealing film 9 is coated over substantially the entire taper portion 22 (the entire region) (see FIG. 8).
  • the sealing film 9 is also coated on the five groove portions 23 formed on the tapered shaft portion 22. That is, the sealing film 9 is disposed in a region of the surface of the abutment 20 where the fixture 10 contacts.
  • the sealing film 9 is coated with a substantially uniform film thickness.
  • the sealing film 9 has a thickness (thickness) of 0.1 ⁇ m to 50 ⁇ m. Preferably, it is 1 ⁇ m to 20 ⁇ m.
  • the sealing film 9 is coated before the abutment 20 is sterilized, and then heat-treated. That is, the abutment 20 on which the sealing film 9 is disposed is ⁇ -ray sterilized and then heated at a temperature of 100 to 300 ° C.
  • the abutment 20 formed of zirconia turns dark brown when subjected to ⁇ -ray sterilization. Thereafter, heat treatment is performed to whiten the abutment 20 and improve aesthetics (see WO2015 / 025656, JP2015039422A1). For this reason, the sealing film 9 is required to have properties (radiation resistance and heat resistance) that do not deteriorate due to ⁇ -ray irradiation and heating.
  • the paraxylylene polymer is suitable as the sealing film 9 because it has radiation resistance and heat resistance.
  • the sealing film 9 is not coated on the part touching the alveolar bone 2. This is because if the sealing film 9 touches the alveolar bone 2, osseointegration with the dental implant 5 may be inhibited. Since the abutment 20 does not touch the alveolar bone 2, the sealing film 9 may be coated on the entire surface of the abutment 20.
  • the sealing film 9 enters the unevenness existing on the surface of the tapered shaft portion 22.
  • the sealing film 9 is made of a polymer of paraxylylene, the sealing film 9 is coated on the surface having fine irregularities with a uniform film thickness and without pinholes.
  • the sealing film 9 is also coated on fine irregularities that are difficult to enter by liquid coating.
  • FIG. 9 is a view showing the clamper pin 30, (a) a side view and (b) a bottom view.
  • the clamper pin 30 is an elongated shaft-shaped member, and is formed of titanium or a titanium alloy.
  • the clamper pin 30 is inserted into the through hole 24 of the abutment 20. Further, the clamper pin 30 engages with the fixture 10.
  • the diameter of the main body 31 of the clamper pin 30 is about 1 mm.
  • a taper portion 32 and an engagement shaft portion 33 are provided on the proximal end side (+ Z side) of the clamper pin 30.
  • the outer diameter of the tapered portion 32 gradually increases (expands) in the + Z direction.
  • the angle of the tapered portion 32 is about 40 °.
  • the tapered portion 32 is accommodated in the reverse tapered hole portion 15 formed in the center hole 13 of the fixture 10.
  • the engaging shaft portion 33 is formed with two outer surfaces (parallel two surfaces 33A) that are parallel to and back from the cylindrical axis.
  • the parallel two surfaces 33A have a width (two surface widths) of about 0.8 mm.
  • the engagement shaft portion 33 is fitted into the engagement hole portion 16 formed at the deepest portion of the center hole 13.
  • a male screw 34 which is a right-hand thread of M1 size, is provided on the tip side ( ⁇ Z side) of the clamper pin 30.
  • the screw dimension of the male screw 34 can be appropriately changed according to the diameter of the main body 31 and the like.
  • the clamper pin 30 is formed in such a length that when the dental implant 5 is assembled, the male screw 34 is exposed (positioned) in the main body side through hole 24A of the through hole 24 of the abutment 20.
  • FIG. 10A and 10B are diagrams showing the clamper 40, where FIG. 10A is a side view, FIG. 10B is a bottom view, and FIG. 10C is a longitudinal sectional view (Xc-Xc cross section).
  • the clamper 40 is a ring-shaped member and is formed of titanium or a titanium alloy.
  • the clamper 40 is fitted to the clamper pin 30.
  • the outer diameter of the clamper 40 is slightly smaller than the minimum inner diameter (the inner diameter of the small diameter portion 15A) of the reverse tapered hole portion 15 of the center hole 13 of the fixture 10.
  • the outer diameter of the clamper 40 is about 1.4 mm, for example.
  • the inner diameter of the clamper 40 is about 1 mm.
  • the clamper 40 is used by being fitted on the clamper pin 30.
  • the clamper 40 is disposed at a position where it is caught by the tapered portion 32 of the clamper pin 30.
  • the clamper 40 is accommodated in the reverse tapered hole portion 15 of the center hole 13 of the fixture 10 when the dental implant 5 is assembled.
  • the outer diameter of the clamper 40 may be formed slightly larger than the minimum inner diameter of the reverse tapered hole portion 15 and may be pushed into the reverse tapered hole portion 15.
  • Eight comb teeth 41 are formed on the base end side (+ Z side) of the clamper 40.
  • the comb teeth 41 are elastically deformed and spread toward the outer peripheral side.
  • the comb teeth 41 of the clamper 40 operate in the same manner as a so-called collet chuck.
  • the maximum outer diameter of the clamper 40 becomes larger than the minimum inner diameter of the tapered hole portion 14 (the inner diameter of the small diameter portion 15A). For this reason, the clamper 40 is caught by the small diameter portion 15 ⁇ / b> A of the reverse tapered hole portion 15. Therefore, movement of the clamper pin 30 with the clamper 40 fitted thereto in the ⁇ Z direction is suppressed.
  • FIG. 11A and 11B are views showing the lock nut 50, where FIG. 11A is a top view and FIG. 11B is a longitudinal sectional view (XIb-XIb cross section).
  • the lock nut 50 is a ring-shaped (cylindrical) member and is formed of titanium or a titanium alloy.
  • the lock nut 50 is inserted into the through hole 24 of the abutment 20 and is screwed into the clamper pin 30.
  • a female screw 52 which is an M1-size right screw, is provided on the inner peripheral surface of the lock nut 50.
  • the screw dimensions and the like of the female screw 52 can be appropriately changed corresponding to the male screw 34.
  • An end face 50A on the base end side (+ Z side) of the lock nut 50 is formed so as to be rotatable around the central axis while abutting (engaging) with the step surface 25 of the through hole 24 of the abutment 20.
  • a straight groove 53 into which a flat-blade screwdriver (not shown) is inserted is provided on the end face 50B on the distal end side ( ⁇ Z side) of the lock nut 50. That is, when the minus driver is engaged with the linear groove 53 and rotated, the lock nut 50 rotates.
  • the lock nut 50 is inserted into the through hole 24 (the main body side through hole 24A) of the abutment 20.
  • a slight gap is provided between the outer peripheral surface 50S of the lock nut 50 and the main body side through hole 24A.
  • the female screw 52 of the lock nut 50 is screwed into the male screw 34 of the clamper pin 30 exposed in the main body side through hole 24A. For this reason, when the lock nut 50 is rotated clockwise while the dental implant 5 is assembled, the end surface 50A of the lock nut 50 comes into contact with and slides against the step surface 25 of the through hole 24 of the abutment 20. At the same time, the clamper pin 30 screwed into the female screw 52 moves in the ⁇ Z direction with respect to the abutment 20.
  • FIG. 12 is a diagram showing the results of a fatigue test of the dental implant 5 (comparison test).
  • FIG. 13 is a diagram showing the results of a fatigue test of the dental implant 5 (endurance test).
  • the vertical axis represents the amplitude (mm) of the repeated load
  • the horizontal axis represents the number of repeated loads (cycle).
  • the dental implants 5A and 5B have the same configuration except for the presence or absence of the sealing film 9.
  • the dental implant 5 ⁇ / b> A is the same as the dental implant 5 described above, and includes a sealing film 9 between the tapered hole portion 14 and the tapered shaft portion 22. Unlike the above-described dental implant 5, the dental implant 5 ⁇ / b> B does not include the sealing film 9 between the tapered hole portion 14 and the tapered shaft portion 22.
  • a fatigue test was performed on the two dental implants 5A and 5B using a fatigue tester compliant with the ISO 14801 standard. Specifically, a load of 200 N was repeatedly applied to the dental implants 5A and 5B at a cycle of 2 Hz. (ISO 14801: 2007 Dental-Implants-Dynamic fatigue test for endosseous dental implants)
  • the fixture 10 and the abutment 20 are each formed of zirconia which is a brittle material. For this reason, when the tapered hole portion 14 and the tapered shaft portion 22 collide with each other, wear powder is generated. The wear powder falls (moves) according to gravity along a slight gap formed between the tapered hole portion 14 and the tapered shaft portion 22. For this reason, the wear powder accumulates on a part of the pressure-resistant part 60 and the rotation preventing part 70. When the abrasion powder accumulates on a part of the pressure-resistant part 60 and the rotation preventing part 70, the external force applied to the pressure-resistant part 60 and the rotation preventing part 70 becomes uneven. In this way, the wear powder causes stress concentration in the pressure-resistant part 60 and the rotation preventing part 70. When stress concentration occurs in ceramics such as zirconia, cracks are generated starting from defects in the material. In the worst case, the crack progresses and leads to breakage.
  • the dental implant 5B was broken by receiving a repeated load of 7173 times.
  • the dental implant 5A includes a sealing film 9.
  • the sealing film 9 is interposed between the tapered hole portion 14 and the tapered shaft portion 22.
  • the sealing film 9 is made of a polymer of paraxylylene, the sealing film 9 is coated with a uniform film thickness and no pinholes on fine irregularities on the surfaces of the tapered hole portion 14 and the tapered shaft portion 22. Is done.
  • the sealing film 9 is also coated on fine irregularities that are difficult to enter by liquid coating.
  • the sealing film 9 encloses (seals) the wear powder inside. That is, the sealing film 9 prevents the wear powder from dropping (moving) according to gravity along a slight gap formed between the tapered hole portion 14 and the tapered shaft portion 22.
  • the film thickness of the sealing film 9 is larger than the particle diameter of the zirconia wear powder. For this reason, the sealing film 9 can reliably contain (seal) the wear powder.
  • the sealing film 9 makes the taper hole part 14 and the taper shaft part 22 contact uniformly, generation
  • the fatigue test of the dental implant 5A was continued (endurance test). As shown in FIG. 13, the dental implant 5A was not damaged even when it was subjected to repeated loading 20 million times. A repeated load of 20 million times corresponds to the number of bites of a person for 100 years. Therefore, after the dental implant 5 (5A) is attached to the alveolar bone 2, there is almost no possibility that the dental implant 5 (5A) is damaged while the person (wearer) is alive.
  • the sealing film 9 brings the tapered hole portion 14 and the tapered shaft portion 22 into uniform contact. This prevents the tapered hole portion 14 and the tapered shaft portion 22 from rubbing (collising) with each other. In other words, the sealing film 9 prevents the generation of wear powder.
  • the sealing film 9 also functions as a layer that prevents generation of wear powder from the tapered hole portion 14 and the tapered shaft portion 22.
  • the dental implant 5 includes a sealing film 9 disposed in the pressure-resistant part 60 (taper shaft part 22, taper hole part 14). For this reason, even if the occlusal pressure F is repeatedly received and abrasion powder is generated from the tapered shaft portion 22 and the tapered hole portion 14, the sealing film 9 encloses (seals) the abrasion powder. Further, in the dental implant 5A, since the tapered hole portion 14 and the tapered shaft portion 22 are in contact with each other through the sealing film 9, generation of wear powder can be prevented.
  • the sealing film 9 is also disposed on the rotation prevention unit 70 (protrusion 17 and groove 23). For this reason, even if the occlusal pressure F is repeatedly received, the abrasion powder generated from the protrusion 17 and the groove 23 is contained (sealed). It is also possible to prevent abrasion powder from being generated from the protrusion 17 and the groove 23.
  • the dental implant 5 can avoid the wear powder from being deposited on a part of the pressure-resistant portion 60 and the rotation preventing portion 70 for a long period of time. Therefore, it is possible to prevent the stress concentration from occurring in the pressure-resistant portion 60 and the rotation preventing portion 70 and the occurrence of cracks in the tapered hole portion 14 and the tapered shaft portion 22. Therefore, the dental implant 5 can prevent damage over a long period of time.
  • the sealing film 9 prevents a meal and the like from entering between the fixture 10 and the abutment 20 during occlusion. For this reason, the dental implant 5 can avoid the intrusion of food residue or the like and becoming unsanitary.
  • the sealing film 9 also prevents ceramic wear powder from being released from the dental implant 5 into the body. Since wear powder generated between the fixture 10 and the abutment 20 is not discharged toward the human body, occurrence of health damage can be avoided. That is, it can be avoided that the ceramic wear powder adversely affects the human body.
  • the sealing film 9 Since the sealing film 9 is coated on the tapered shaft portion 22 of the abutment 20 by a chemical vapor deposition method, the sealing film 9 can be uniformly fixed over the entire tapered shaft portion 22 (over the entire area). For this reason, the function of the sealing film 9 can fully be exhibited. Since a polymer of paraxylylene is used for the sealing film 9, it is safe for the human body and is excellent in wear resistance, chemical resistance, insulation, and moisture resistance.
  • the film thickness (thickness) of the sealing film 9 is 0.1 ⁇ m or more and 50 ⁇ m or less. Preferably, they are 1 micrometer or more and 20 micrometers or less.
  • the particle size of the zirconia wear powder is 0.1 ⁇ m or less. For this reason, the film thickness of the sealing film 9 is thicker than the particle size of the wear powder. Therefore, the sealing film 9 can reliably contain (seal) the wear powder. Even if the particle size of the wear powder is larger than the film thickness of the sealing film 9, since most of the wear powder is covered with the sealing film 9, the movement of the wear powder is prevented.
  • FIG. 14 is a diagram showing an artificial hip joint implant 105 according to an embodiment of the present invention.
  • the artificial hip joint implant (implant) 105 includes a pelvic component 106 fixed to the pelvis (bone) 102, and a femoral component 107 slidably contacting the pelvic component 106.
  • the femoral component 107 is fixed to the femur (bone) 103.
  • a pelvic component (implant body, proximal bone component) 106 has a cup 106 a that is recessed in a spherical shape, and is fixed to the pelvis 102.
  • the femoral component (connector, distal bone component) 107 has a stem 107a embedded in the femur 103 and a head 107b that protrudes spherically from the stem 107a and slides against the cup 106a.
  • the cup (contacted portion, sliding contact portion) 106a and the head (contact portion, sliding contact portion) 107b are each formed of a ceramic material such as zirconia.
  • the sealing film 9 is coated on the surfaces of the cup 106a and the head 107b.
  • the sealing film 9 contains (seals) the wear powder. Further, since the cup 106a and the head 107b are in contact with each other through the sealing film 9, the generation of wear powder can be prevented. Therefore, accumulation between the cup 106a and the head 107b can be avoided over a long period of time, and cracks can be prevented from occurring in the cup 106a and the head 107b. Therefore, the artificial hip joint implant 105 can prevent damage over a long period of time.
  • the sealing film 9 prevents the release of ceramic wear powder, the occurrence of health damage can be prevented.
  • FIG. 15 is a diagram showing an artificial knee joint implant 115 according to an embodiment of the present invention.
  • the artificial knee joint implant (implant) 115 includes a femoral component 116 fixed to the femur (bone) 112, and a tibial component 117 slidably contacting the femoral component 116.
  • the tibial component 117 is fixed to the tibia 113.
  • the femoral component (implant body, proximal bone component) 116 has a head 116 a protruding in an arc shape and is fixed to the femur 112.
  • the tibial component (connector, distal bone component) 117 includes a base 117a embedded in the tibia 113 and a cup 117b that is connected to the base 117a and is recessed in an arc shape.
  • the cup 117b is in sliding contact with the head 116a.
  • the base 117a and the cup 117b may be integrally formed.
  • the head (contacted portion, sliding contact portion) 116a and the cup (contacting portion, sliding contact portion) 117b are each formed of a ceramic material such as zirconia.
  • the sealing film 9 is coated on the surfaces of the head 116a and the cup 117b.
  • the sealing film 9 contains (seals) the wear powder. That is, the same effect as the artificial hip joint implant 105 is exhibited. Therefore, the artificial knee joint implant 115 can prevent damage over a long period of time. In addition, since the sealing film 9 prevents the release of ceramic wear powder, the occurrence of health damage can be prevented.
  • FIG. 16 is a diagram showing an artificial shoulder joint implant 125 according to an embodiment of the present invention.
  • the shoulder prosthesis implant (implant) 125 includes a scapula component 126 fixed to the scapula (bone) 122, and a humerus component 127 that slides against the scapula component 126.
  • the humerus component 127 is fixed to the humerus 123.
  • the scapula component (implant body, proximal bone component) 126 has a cup 126 a that is recessed in an arc shape, and is fixed to the scapula 122.
  • the humerus component (connector, distal bone component) 127 has a stem 127a embedded in the humerus 123 and a head 127b that protrudes spherically from the stem 127a and slides against the cup 126a.
  • the cup (contacted portion, sliding contact portion) 126a and the head (contact portion, sliding contact portion) 127b are each formed of a ceramic material such as zirconia.
  • the sealing film 9 is coated on the surfaces of the cup 126a and the head 127b.
  • the sealing film 9 contains (seals) the wear powder. That is, the same effects as the artificial hip joint implant 105 and the like are exhibited. Therefore, the shoulder prosthesis implant 125 can prevent damage over a long period of time. In addition, since the sealing film 9 prevents the release of ceramic wear powder, the occurrence of health damage can be prevented.
  • FIG. 17 is a diagram showing an inverted shoulder prosthesis implant 135 according to an embodiment of the present invention.
  • An inverted shoulder prosthesis implant (implant) 135 is obtained by replacing the cup 126a and the head 127b in the shoulder prosthesis implant 125.
  • the cup (contact part, sliding contact part) 126a slides (contacts) with the head (contacted part, sliding contact part) 127b, and wear powder is generated. Even so, the sealing film 9 encloses (seals) the abrasion powder. That is, the same effect as the artificial shoulder joint implant 125 is exhibited. Therefore, the inverted shoulder prosthesis implant 135 can be prevented from being damaged over a long period of time. In addition, since the sealing film 9 prevents the release of ceramic wear powder, the occurrence of health damage can be prevented.
  • FIG. 18 is a diagram illustrating an artificial elbow joint implant 145 according to an embodiment of the present invention.
  • the artificial elbow joint implant (implant) 145 includes a humeral component 146 that is fixed to the humerus (bone) 142, and a radial component 147 that is in sliding contact with the humeral component 146.
  • the rib component 147 is fixed to the rib 143.
  • the humerus component (implant body, proximal bone component) 146 includes a stem 146a embedded in the humerus 142 and a cup 146b that is connected to the stem 146a and is recessed in an arc shape.
  • the stem 146a and the cup 146b may be integrally formed.
  • the rib component (connector, distal bone component) 147 has a head 147 a protruding in an arc shape and is fixed to the rib 143.
  • the head 147a is in sliding contact with the cup 146b.
  • the cup (contacted portion, sliding contact portion) 146b and the head (contact portion, sliding contact portion) 147a are each formed of a ceramic material such as zirconia.
  • the sealing film 9 is coated on the surfaces of the cup 146b and the head 147a.
  • the sealing film 9 contains (seals) the wear powder. That is, the same effect as the artificial hip joint implant 105 is exhibited. Therefore, the artificial elbow joint implant 145 can prevent damage over a long period of time. In addition, since the sealing film 9 prevents the release of ceramic wear powder, the occurrence of health damage can be prevented.
  • FIG. 19 is a diagram showing an artificial ankle implant 155 according to an embodiment of the present invention.
  • the artificial ankle implant (implant) 155 includes a tibial component 156 that is fixed to the tibia (bone) 152, and a talus component 157 that slides against the tibial component 156.
  • Talar component 157 is secured to talar 153.
  • the tibial component (implant body, proximal bone component) 156 has a cup 156 a that is recessed in an arc shape, and is fixed to the tibia 152.
  • the talar component (connector, distal bone component) 157 has a head 157a protruding in an arc shape, and is fixed to the talar 153.
  • the head 157a is in sliding contact with the cup 156a.
  • the cup (contacted part, sliding contact part) 156a and the head (contacting part, sliding contact part) 157a are each formed of a ceramic material such as zirconia.
  • the sealing film 9 is coated on the surfaces of the cup 156a and the head 157a.
  • the sealing film 9 encloses (seals) the abrasion powder. That is, the same effect as the artificial hip joint implant 105 is exhibited. Therefore, the artificial ankle implant 155 can prevent damage over a long period of time. In addition, since the sealing film 9 prevents the release of ceramic wear powder, the occurrence of health damage can be prevented.
  • the fixture 10 does not have to have the tapered hole portion 14 and the abutment 20 has the tapered shaft portion 22.
  • the case where the fixture 10 has the taper shaft part 22 and the abutment 20 has the taper hole part 14 may be sufficient.
  • the sealing film 9 is not limited to being fixed to the tapered shaft portion 22 of the abutment 20.
  • positions only in the taper hole 14 of the fixture 10 may be sufficient.
  • the sealing film 9 only needs to be disposed in the pressure-resistant portion 60 (tapered hole portion 14, tapered shaft portion 22), and may be removable from the tapered hole portion 14 and the tapered shaft portion 22.
  • the sealing film 9 is not limited to the case where the sealing film 9 is disposed on both the pressure-resistant portion 60 and the rotation preventing portion 70 (the protrusion 17 and the groove portion 23). The sealing film 9 only needs to be disposed in the pressure-resistant portion 60.
  • the proximal bone component such as the pelvic component 106 corresponds to the implant body
  • the distal bone component such as the femoral component 107 corresponds to the connection body
  • the connection body may be a case where it is fixed to the bone in the same manner as the implant body.
  • the proximal bone component may correspond to a connection body
  • the distal bone component may correspond to an implant body.
  • the cup 106a and the like may be called a bone receiver, a socket, an acetabular shell, a grenoid, or the like.
  • the head 107b or the like may be called a bone head, a ball, a genosphere, or the like.
  • the sealing film 9 is not limited to being disposed on both the cup 106a and the head 107b and the like. It may be arranged only in the cup 106a or the like, or may be arranged only in the head 107b or the like. The sealing film 9 may be removable from the cup 106a and the head 107b and the like.
  • the sealing body is not limited to a film-like form (sealing film 9).
  • the sealing body may be in a form other than the film.
  • the sealing body may be in the form of, for example, a sheet, a tape, a string, a granule, or a powder.
  • the fixture 10 of the dental implant 5, the abutment 20, the cup 106a of the hip implant 105, the head 107b, and the like are not limited to being formed of zirconia (zirconium oxide).
  • These members may be biocompatible ceramic materials such as alumina (aluminum oxide), yttrium oxide, hafnium oxide, silicone oxide, magnesium oxide, and cerium oxide. May be formed.
  • Either the fixture 10 or the abutment 20 may be formed of a metal material such as titanium or a titanium alloy.
  • the abrasion powder generated from the tapered hole portion 14 can be sealed by disposing the sealing film 9 in the tapered hole portion 14.
  • the wear powder generated from the tapered hole portion 14 can be sealed by disposing the sealing film 9 on the tapered shaft portion 22.
  • the abrasion powder generated from the tapered shaft portion 22 can be sealed by disposing the sealing film 9 in the tapered hole portion 14.
  • the abrasion powder generated from the tapered shaft portion 22 can be sealed by disposing the sealing film 9 on the tapered shaft portion 22.
  • Either the proximal bone component (such as the pelvic component 106) or the distal bone component (such as the femoral component 107) may be formed of a metal material such as titanium or a titanium alloy.
  • either one of the sliding contact portion (cup 106a or the like) or the sliding contact portion (head 107b or the like) may be formed of a metal material.
  • the wear powder generated from the sliding contact portion can be sealed by disposing the sealing film 9 on the sliding contact portion.
  • the wear powder generated from the sliding contact portion can be sealed by disposing the sealing film 9 on the sliding contact portion.
  • the wear powder generated from the sliding contact portion can be sealed by disposing the sealing film 9 on the sliding contact portion.
  • the wear powder generated from the sliding contact portion can be sealed by disposing the sealing film 9 on the sliding contact portion.
  • the artificial joint implant may be placed in a joint such as a wrist, a finger joint, or a temporomandibular joint in addition to a hip joint.
  • Implants are not limited to humans, and may be applied to pets such as dogs and cats and livestock such as cows and horses.

Abstract

L'invention concerne un implant (5) qui comprend : un corps d'implant en céramique (10) qui est fixé à un os (2); un corps de liaison en céramique (20) ayant une partie de contact (22) qui entre en contact avec une partie (14) à mettre en contact formée dans le corps d'implant (10); et un corps d'étanchéité (9) qui est disposé entre la partie de contact (22) et la partie (14) à mettre en contact, et qui scelle une poudre d'abrasion formée à partir de la partie de contact (22) et de la partie (14) à mettre en contact. Le corps d'étanchéité est disposé dans une zone qui n'entre pas en contact avec l'os (2). Le corps d'étanchéité (9) est fixé à la partie (14) à mettre en contact et/ou la partie de contact (22).
PCT/JP2015/068950 2015-07-01 2015-07-01 Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe WO2017002223A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2016501909A JPWO2017002223A1 (ja) 2015-07-01 2015-07-01 インプラント、フィクスチャー、アバットメント
PCT/JP2015/068950 WO2017002223A1 (fr) 2015-07-01 2015-07-01 Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2015/068950 WO2017002223A1 (fr) 2015-07-01 2015-07-01 Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe

Publications (1)

Publication Number Publication Date
WO2017002223A1 true WO2017002223A1 (fr) 2017-01-05

Family

ID=57608310

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2015/068950 WO2017002223A1 (fr) 2015-07-01 2015-07-01 Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe

Country Status (2)

Country Link
JP (1) JPWO2017002223A1 (fr)
WO (1) WO2017002223A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2023012410A (ja) * 2021-07-13 2023-01-25 ユニデンタル カンパニー リミテッド パリレンを用いたインプラントのコーティング方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3865138B2 (ja) * 2002-06-10 2007-01-10 一穂 家坂 関節包付き人工関節
WO2007116690A1 (fr) * 2006-03-29 2007-10-18 Japan Medical Materials Corporation biomateriau, articulation artificielle utilisant ledit biomateriau et procede de production
WO2009044816A1 (fr) * 2007-10-03 2009-04-09 Japan Medical Materials Corporation Matériau biocompatible et hautement résistant à l'usure, articulation artificielle l'utilisant et leur procédé de production
JP2012152453A (ja) * 2011-01-27 2012-08-16 Sekisui Chem Co Ltd 人工関節

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102010051176A1 (de) * 2010-11-15 2012-05-16 Urs Brodbeck Dental-Implantatsystem und Verfahren zur Herstellung eines Dental-Implantatsystems
JP2013244216A (ja) * 2012-05-25 2013-12-09 Nanto Precision Co Ltd インプラント及びアバットメント体
WO2014007959A1 (fr) * 2012-07-02 2014-01-09 Icon Medical Corp. Alliage métallique amélioré pour dispositifs médicaux

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3865138B2 (ja) * 2002-06-10 2007-01-10 一穂 家坂 関節包付き人工関節
WO2007116690A1 (fr) * 2006-03-29 2007-10-18 Japan Medical Materials Corporation biomateriau, articulation artificielle utilisant ledit biomateriau et procede de production
WO2009044816A1 (fr) * 2007-10-03 2009-04-09 Japan Medical Materials Corporation Matériau biocompatible et hautement résistant à l'usure, articulation artificielle l'utilisant et leur procédé de production
JP2012152453A (ja) * 2011-01-27 2012-08-16 Sekisui Chem Co Ltd 人工関節

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2023012410A (ja) * 2021-07-13 2023-01-25 ユニデンタル カンパニー リミテッド パリレンを用いたインプラントのコーティング方法
JP7420399B2 (ja) 2021-07-13 2024-01-23 ユニデンタル カンパニー リミテッド インプラントのコーティング方法

Also Published As

Publication number Publication date
JPWO2017002223A1 (ja) 2017-07-13

Similar Documents

Publication Publication Date Title
JP5543484B2 (ja) 歯インプラント
JP5096339B2 (ja) ２部分から成る歯インプラント
US20210015589A1 (en) Dental implant with improved prosthetic interface
KR101808599B1 (ko) 치과용 임플란트
Alexandre Gehrke et al. Misfit of Three Different Implant-Abutment Connections Before and After Cyclic Load Application: An In Vitro Study.
US9788920B2 (en) Endosseous implant having improved anchorage
Yao et al. Mechanical performance of conical implant-abutment connections under different cyclic loading conditions
TW201225930A (en) Implant, implant object, abutment object
JP2009527339A (ja) セラミック／金属製の歯科用アバットメント
WO2017002223A1 (fr) Implant, corps d'implant, butée, élément osseux côté extrémité de base, et élément osseux côté extrémité de pointe
WO2003030767A1 (fr) Dispositif de fixation et de montage conçus pour une operation d'implantation
WO2015186123A1 (fr) Système universel de fixation d'un implant sur un os
JP5449292B2 (ja) ２部分から成る歯インプラント
JP6917090B2 (ja) 医療用デバイス
JP2013244216A (ja) インプラント及びアバットメント体
RU196535U1 (ru) Телескопический фиксатор-абатмент для вторичной конструкции из полиэфирэфиркетона
RU195904U1 (ru) Дентальный имплантат
JP2006296558A (ja) 生体インプラント材
WO2020055352A2 (fr) Implant dentaire constitué de matériau peek
RU2482813C2 (ru) Унитарный зубной имплантат
Kim et al. Application of finite element analysis to evaluate implant fractures
JP2013244215A (ja) インプラント及びアバットメント体
GB2516662A (en) Hip and knee joint prostheses
JP2011217911A (ja) 歯科用インプラントのフィクスチャー

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 2016501909

Country of ref document: JP

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 15897150

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 15897150

Country of ref document: EP

Kind code of ref document: A1