US20050106534A1 - Ceramic dental implant - Google Patents
Ceramic dental implant Download PDFInfo
- Publication number
- US20050106534A1 US20050106534A1 US10/496,814 US49681404A US2005106534A1 US 20050106534 A1 US20050106534 A1 US 20050106534A1 US 49681404 A US49681404 A US 49681404A US 2005106534 A1 US2005106534 A1 US 2005106534A1
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- United States
- Prior art keywords
- anchoring part
- dental implant
- anchoring
- coating
- implant
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Classifications
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- 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
- A61C8/0012—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy
-
- 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
- A61C8/0012—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy
- A61C8/0013—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy with a surface layer, coating
- A61C8/0015—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy with a surface layer, coating being a conversion layer, e.g. oxide layer
-
- 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
- A61C8/0012—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy
- A61C8/0013—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the material or composition, e.g. ceramics, surface layer, metal alloy with a surface layer, coating
-
- 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
- A61C8/0018—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the shape
- A61C8/0022—Self-screwing
-
- 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
- A61C8/0048—Connecting the upper structure to the implant, e.g. bridging bars
- A61C8/005—Connecting devices for joining an upper structure with an implant member, e.g. spacers
- A61C8/0066—Connecting devices for joining an upper structure with an implant member, e.g. spacers with positioning means
-
- 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
- A61C8/0048—Connecting the upper structure to the implant, e.g. bridging bars
- A61C8/005—Connecting devices for joining an upper structure with an implant member, e.g. spacers
- A61C8/0069—Connecting devices for joining an upper structure with an implant member, e.g. spacers tapered or conical connection
-
- 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
- A61C8/0048—Connecting the upper structure to the implant, e.g. bridging bars
- A61C8/0075—Implant heads specially designed for receiving an upper structure
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/53—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone involving the removal of at least part of the materials of the treated article, e.g. etching, drying of hardened concrete
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
- C04B41/91—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics involving the removal of part of the materials of the treated articles, e.g. etching
-
- 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
- A61C8/0018—Means to be fixed to the jaw-bone for consolidating natural teeth or for fixing dental prostheses thereon; Dental implants; Implanting tools characterised by the shape
- A61C8/0037—Details of the shape
- A61C2008/0046—Textured surface, e.g. roughness, microstructure
-
- 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
- A61C8/0089—Implanting tools or instruments
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00836—Uses not provided for elsewhere in C04B2111/00 for medical or dental applications
Definitions
- the invention relates to a dental implant comprising an anchoring part for anchoring within the bone and comprising a mounting part for receiving an element to be attached, such as an abutment or a crown, a bridge or a prosthesis construction.
- Dental implants have been successfully used since more than 10 years.
- the major part of the dental implants currently used consist of titanium, since titanium has a sufficiently low elastic modulus and also has a relatively large strength.
- a safe integral osteogenesis can be reached when the surface is suitably treated (e.g. roughened by sand blasting).
- the titanium implants after reaching a primary stability by screwing into the bone, safely ossify within a healing time of about 3 to 4 months so that a permanent bond between the anchoring part screwed into the bone and the bone is guaranteed.
- two-part implants are utilized. Basically, there are two possibilities for this end:
- the anchoring part of the implant is embedded until the bone ridge so that the mucoperiost cover can be sewn above the implant.
- a drawback is the necessary secondary operation at the end of the primary healing phase for allowing a subsequent application of a mounting part and thereon the desired prosthesis or crown.
- the anchoring part of the implant can be sunk in up to about 3 mm above the bone ridge at mucosal level, thus avoiding a secondary operation.
- the wound edges can be directly adapted to the implant neck portion, thereby effecting a primary soft tissue closure to the implant.
- Such a two-part implant construction for an open transgingival system is e.g. marketed by Institut-Straumann AG, Waldenburg/Switzerland under the mark ITI®DENTAL IMPLANT SYSTEM.
- Both the anchoring or primary part which is implanted transgingivally, as well as the assigned construction parts herein consist of pure titanium.
- the titanium surface is either coarsely sand blasted or is coated with titanium by thermal spraying. Both surfaces guarantee a good ossification or integrating osteogenesis.
- Ceramic abutments offer particular advantages during the subsequent matching of the supra-construction, such as bridges or crowns, to the abutment, They can be simply ground and allow to build constructions using prior art processes known to the dentist. Ceramic abutments offer particular advantages due to the fact that their color can be closely matched to the natural tooth color. Lately also abutments of zirconia have been developed which offer a particularly high strength.
- Such a system consisting of two-part implants having an anchoring part and a mounting part, an abutment and a prosthesis applied thereon offers a good matching to the geometric situation for different indications, however, generally the multitude of the components used is detrimental for the mechanical stability of the total system. Also each further bonding leads to possible starting points for bacteria which may cause parodontitis or gingivitis within the gap.
- zirconia ceramics have become available that have an extremely high strength, in particular when the shaped bodies are prepared by hot isostatic pressing or by subsequent hot isostatic densifying,
- Such a zirconia ceramic which may roughly comprise 92.1-93.5 wt.-% ZrO 2 , 4.5-5.5 wt.-% Y 2 O 3 and 3.8-2.2 wt.-% HfO 2 , is for instance known from U.S. Pat. No. 6,165,925.
- zirconia ceramic as a material for making the anchoring part of an implant seems not possible, since a sufficient mechanical stability of the zirconia ceramic is necessary, this requiring a highly dense preparation, practically without any porosity to be measured, this simultaneously leading to a clean cut extremely hard surface.
- Such a material is bio-inert, so that no integrating osteogenesis is to be expected, this is why this material is not regarded to be suitable for the preparation of an anchoring part of an implant.
- a dental implant comprising an anchoring part for anchoring within the bone, and comprising a mounting part for receiving an element to be applied, wherein the anchoring part and the mounting part are integrally made of a material based on zirconia, and wherein at least the anchoring part is pre-treated at its outer surface by a subtractive removing process, or is provided with a coating, whereby an ossification is facilitated.
- this object is achieved by a process for making a dental implant, wherein initially a base body having an anchoring part for anchoring within the bone and a mounting part for receiving an element to be applied, is provided integrally from a material based on zirconia, and wherein subsequently at least the anchoring part is pre-treated at its outer surface at least partially by a subtractive, removing process or is coated with a coating that facilitates ossification.
- a one-part dental implant having an anchoring part and a mounting part can be prepared that consists of a material based on zirconia and which still guarantees a good ossification during healing time.
- the mounting part can be approximated to the natural tooth color and thus in particular in the visible region allows the preparation of completely natural looking ceramic reconstructions.
- the mounting part can be directly ground which allows a simple and advantageous adaptation of the additional elements to be applied. Possibly additional abutments may become superfluous.
- DE 28 38 759 A1 it is basically known to provide an implant consisting of metal, plastic or ceramic with a layer system consisting of a passivating layer and/or of several physiologically active layers.
- a passivating layer of silicon nitride and a physiologically active layer of calcium fluoride, of ⁇ -alanin, of carbon or the like is contemplated.
- the implant according to the invention is applied transgingivally.
- the soft tissue attachment developing the biological breadth is not disturbed by a secondary operation such as occurring with systems that heal with covered mucous linings.
- a primary treatment by applying a temporary measure directly onto the mounting part is made possible.
- a sufficient primary stability e.g. by screwing the anchoring part into a bone bore
- only measures must be taken to avoid in particular sharing motions during the subsequent healing time.
- this can be effected by a blocking, while with single implants this can be effected by an attachment to adjacent teeth or to prosthetic parts partially by applying adhesive.
- the anchoring part comprises a threaded section.
- the implant according to the invention can be implanted with the necessary primary stability so that subsequently to the implantation directly a primary treatment is made possible by applying a temporary measure.
- the anchoring part at its outer surface is at least partially roughened by a removing process or is micro-structured.
- Such a surface structuring guarantees that the zirconium oxide material which would otherwise be bio-inert can reach an integral osteogenesis with the bone material.
- the dental implant in the region of the anchoring part has a maximum surface roughness between 1 and 20 ⁇ m, preferably between 2 and 15 ⁇ m, in particular between 4 and 12 ⁇ m, particularly preferred between 6 and 12 ⁇ m.
- an abrasive blasting such as sand blasting (using corundum), a blasting with boron carbide particles, or a high-pressure water blasting, is possible.
- abrasive blasting such as sand blasting (using corundum)
- a blasting with boron carbide particles or a high-pressure water blasting
- a hard material for blasting such as boron carbide particles which is considerably costly, however.
- an initial blasting treatment such as sand blasting with Al 2 O 3
- a subsequent etching treatment using phosphoric acid, sulphuric acid, hydrochloric acid or mixtures thereof.
- the blasting treatment may be performed using a pressure between about 1 bar and 10 bars, preferably between 2 and 6 bars, in particular between 3 and 5 bars.
- an etching treatment is desired using phosphoric acid of 10 to 90 vol.-%, preferably of 15 to 50 vol.-%, in particular of 20 to 40 vol.-%.
- the etching may e.g. be performed for a time of 10 seconds to 10 minutes, preferably between 10 and 120 seconds, in particular between about 15 to 60 seconds.
- the etching treatment suitably is followed by a cleaning step, such as rinsing within a NaCl solution and subsequent rinsing in deionized water.
- the anchoring part at its outer surface is at least partially provided with a bio-active coating.
- This may for instance be a silanizing or a hydroxylation which also facilitates osteogenesis
- the anchoring part is at least partially coated with a metallic or ceramic coating or with a cermet coating.
- the anchoring part may e.g. be coated by thermal spraying, by CVD or by PVD.
- a coating consisting of titanium or of a titanium alloy is regarded as advantageous, which possibly may be applied by thermal spraying.
- the bio-compatibility of titanium having been known since years, can be utilized for reaching a safe integral osteogenesis of the anchoring part during the healing phase.
- the titanium possibly applied by thermal spraying has a sufficient micro-structuring to avoid a distant osteogenesis and to guarantee a safe ossification.
- the region within the anchoring part is coated that will be recessed within the bone during implantation.
- the advantageous aesthetics of the zirconia-based ceramic in the region of the mounting part can be combined with the advantageous bio-compatibility of titanium.
- the mounting part comprises a support for applying a screwing tool.
- the mounting part may be designed for positive fitting of a screwing tool, such as basically already known in the art.
- the dental implant can be designed with all kinds of implant shapes already known or to be developed.
- the mounting part may be configured as an extension of the anchoring part or may be offset with respect to the anchoring part.
- the mounting part may have a frusto-conical basic shape, this facilitating an adhesive attachment of abutments for prosthesis constructions.
- the dental implant is stored in a suitable liquid, such as deionized water, after a previous activation of its surface, such as by silanizing or hydroxylation or by an etching treatment, before it is implanted by the doctor.
- a suitable liquid such as deionized water
- the dental implant may be stored within a container, preferably without air access.
- a zirconia ceramic prepared in this way may for instance be processed by grinding to the desired shape of the dental implant and may be subsequently surface-treated to reach the desired surface characteristics.
- FIG. 1 a side view of a first embodiment of an implant according to the invention
- FIG. 2 a side view of an embodiment of an implant according to the invention slightly modified with respect to the embodiment of FIG. 1 ;
- FIG. 3 a side view of a further embodiment of an implant according to the invention wherein the mounting part is slightly offset with respect to the anchoring part;
- FIG. 4 a REM photograph of a test specimen of an implant which has been implanted into a patient and which has been removed together with the adjacent bone material using a drill after a healing period of about 3 months.
- FIGS. 1-3 several possible embodiments of a one-part dental implant according to the invention are depicted, this being purely exemplary without limiting the scope of the invention to any kind of shape of the implant.
- a dental implant according to the invention is designated in total with numeral 10 . It comprises an anchoring part 12 having a threaded section 14 and a rounded lower end.
- the anchoring part 12 at its upper end transitions via a slightly enlarged conical section 16 to the outside into a mounting part 18 being integral therewith and extending within an extension of the longitudinal axis 24 of the threaded section 14 .
- the mounting part 18 has a frusto-conical or a conical shape and is provided with a flattening 20 at one side thereof. At the side opposite the flattening 20 there is provided a groove 22 within the outer surface that extends from the upper front surface of the mounting part 18 toward the lower side and ends in a conical section which forms the transition to the conical section 16 of the anchoring part 12 .
- the flattening 20 in combination with the groove 22 located on the opposite side functions to provide a positive attachment of a screwing tool which has a plug-in seat matched thereto.
- FIG. 2 shows a slightly modified embodiment of a dental implant designated in total with numeral 30 which again comprises an anchoring part 32 having a threaded section 34 being followed by a conical mounting part 38 on which the groove 42 can be seen, since the dental implant 30 is depicted rotated by 90° with respect to the dental implant 10 of FIG. 1 .
- the dental implant 30 does not have a conical section within the transitional region between the anchoring part 32 and the mounting part 38 .
- the mounting part 38 is configured as a conical section directly adjoining the anchoring part 32 which is shaped cylindrically. Again on the side opposite to the groove 42 a respective flattening may be provided, such as can be seen in FIG. 1 .
- FIG. 3 a modified embodiment of the dental implant is designated in total with numeral 50 .
- the dental implant 50 comprises an anchoring part 52 corresponding to the embodiment according to FIG. 1 and having a threaded section 54 which transitions via an outer conical section 56 into a mounting part 58 .
- the mounting part 58 has a conical basic shape, however, is offset with respect to the longitudinal axis of the anchoring part 52 , e.g. by an angle of about 15°, this being particularly suitable for applications within the incisor region in many cases.
- a suitable recess 60 at the outer surface of the mounting part 58 a positive engagement of a screwing tool is made possible to also allow to screw into a bone bore this dental implant having an offset mounting part.
- the anchoring part may e.g. have an axial length of 10 mm, wherein the other dimensions result in a corresponding manner.
- the dimensions and the shane may be modified in a suitable way, depending on the respective indication.
- the dental implants 10 , 30 , 50 according to the invention are prepared integrally from a zirconia ceramic which e.g. may be a stabilized zirconia ceramic having 92.1 to 93.5 wt.-% ZrO 2 and 4.5 to 5.5 wt.-% Y 2 O 3 and 1.8 to 2.2 wt.-% HfO 2 according to U.S. Pat. No. 6,165,925 mentioned at the outset.
- a stabilized zirconia ceramic in particular, when prepared by hot isostatic pressing or by sintering with subsequent hot isostatic densification offers a particularly high mechanical stability and strength. Also the utilization of any other zirconia ceramics is conceivable.
- the anchoring part at its outer surface thereof has been treated by a suitable removing pretreatment or by a suitable coating to thereby reach a good integral osteogenesis after implantation.
- the anchoring part may be silanated or hydroxylated or may be roughened by a removing process or may be micro-structured.
- an integral osteogenesis can be reached.
- a coating by thermal spraying consisting of pure titanium having a layer thickness of about 20 to 100 ⁇ m.
- a safe integral osteogenesis can be reached during healing time, wherein simultaneously the advantages of zirconia ceramic, such as grinding possibility and a color approximated to the natural tooth can be utilized.
- test implant samples according to FIG. 4 were prepared from a zirconia ceramic according to U.S. Pat. No. 6,165,925 and were processed by grinding to yield the shape according to FIG. 4 .
- the test implant sample 70 shown in FIG. 4 was implanted into a patient. After a healing time of about 3 months the test implant sample was removed together with a small amount of the surrounding bone material using a hollow drill and was analyzed histologically with respect to osteointegration. It was found that an integrating osteogenesis can be reached.
- Additional improvements with respect to an integrating osteogenesis already after short healing time are particularly expected when using increased surface roughnesses in the range of about 5 to 15 ⁇ m R max to which end in particular a subsequent treatment of the blasted surface by etching with phosphoric acid is contemplated.
- the surface roughness can be increased to 5 to 15 ⁇ m R max (in particular to about 8 to 12 ⁇ m, depending on the previous blasting treatment).
- the activation of the surface reached by etching facilitates an osteointegration.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/407,262 US20090176191A1 (en) | 2001-11-30 | 2009-03-19 | Ceramic dental implant |
US13/228,642 US10271927B2 (en) | 2001-11-30 | 2011-09-09 | Ceramic dental implant |
US14/978,781 US20160106524A1 (en) | 2001-11-30 | 2015-12-22 | Ceramic dental implant |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10159683A DE10159683A1 (de) | 2001-11-30 | 2001-11-30 | Dantalimplantat |
DE10159683.9 | 2001-11-30 | ||
PCT/EP2002/013187 WO2003045268A1 (fr) | 2001-11-30 | 2002-11-23 | Implant dentaire céramique |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2002/013187 A-371-Of-International WO2003045268A1 (fr) | 2001-11-30 | 2002-11-23 | Implant dentaire céramique |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/407,262 Division US20090176191A1 (en) | 2001-11-30 | 2009-03-19 | Ceramic dental implant |
US13/228,642 Division US10271927B2 (en) | 2001-11-30 | 2011-09-09 | Ceramic dental implant |
Publications (1)
Publication Number | Publication Date |
---|---|
US20050106534A1 true US20050106534A1 (en) | 2005-05-19 |
Family
ID=7708100
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/496,814 Abandoned US20050106534A1 (en) | 2001-11-30 | 2002-11-23 | Ceramic dental implant |
US12/407,262 Abandoned US20090176191A1 (en) | 2001-11-30 | 2009-03-19 | Ceramic dental implant |
US13/228,642 Active 2024-05-18 US10271927B2 (en) | 2001-11-30 | 2011-09-09 | Ceramic dental implant |
US14/978,781 Abandoned US20160106524A1 (en) | 2001-11-30 | 2015-12-22 | Ceramic dental implant |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/407,262 Abandoned US20090176191A1 (en) | 2001-11-30 | 2009-03-19 | Ceramic dental implant |
US13/228,642 Active 2024-05-18 US10271927B2 (en) | 2001-11-30 | 2011-09-09 | Ceramic dental implant |
US14/978,781 Abandoned US20160106524A1 (en) | 2001-11-30 | 2015-12-22 | Ceramic dental implant |
Country Status (8)
Country | Link |
---|---|
US (4) | US20050106534A1 (fr) |
EP (5) | EP1779807A1 (fr) |
JP (5) | JP2006501867A (fr) |
AT (3) | ATE304328T1 (fr) |
AU (1) | AU2002356716A1 (fr) |
DE (3) | DE10159683A1 (fr) |
ES (4) | ES2661336T3 (fr) |
WO (1) | WO2003045268A1 (fr) |
Cited By (62)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050113834A1 (en) * | 2003-10-27 | 2005-05-26 | Michael Breitenstien | Implant with a ceramic coating, and method for ceramic coating of an implant |
US20050170311A1 (en) * | 2002-02-28 | 2005-08-04 | Philippe Tardieu | Method and device for placing dental implants |
US20060093988A1 (en) * | 2003-02-28 | 2006-05-04 | Swaelens Bart F J | Method for placing and manufacturing a dental superstructure, method for placing implants and accessories used thereby |
US20060246399A1 (en) * | 2005-03-16 | 2006-11-02 | Ehrl Peter A | Two-part ceramic dental implant |
US20070068827A1 (en) * | 2003-10-16 | 2007-03-29 | Vincent Jemelin | Cyclic olefin copolymer external capsule for preserving medical device |
US20070099152A1 (en) * | 2005-10-31 | 2007-05-03 | Albert Busch | Dental implant system |
US20070160953A1 (en) * | 2003-12-01 | 2007-07-12 | Philippe Tardieu | Method for manufacturing a prosthesis made prior to implant placement |
EP1825830A1 (fr) * | 2006-02-28 | 2007-08-29 | Straumann Holding AG | Implant de deux pièces avec une surface hydroxylée pour venir en contact avec un tissu mou |
EP1825828A1 (fr) * | 2006-02-28 | 2007-08-29 | Straumann Holding AG | Implant d'une seule pièce avec une surface hydroxylée pour venir en contact avec un tissu mou |
EP1825829A1 (fr) * | 2006-02-28 | 2007-08-29 | Straumann Holding AG | Tenon avec une surface hydroxylée |
US20080090208A1 (en) * | 2006-10-16 | 2008-04-17 | Natural Dental Implants Gmbh | Customized dental prosthesis for periodontal- or osseointegration, and related systems and methods |
US20080213728A1 (en) * | 2005-07-11 | 2008-09-04 | Ill-Mo Rhew | Dental Implant Fixture |
US20080213725A1 (en) * | 2003-09-24 | 2008-09-04 | Nobel Biocare Ab (Publ) | Method and Arrangement for a Dental Installation |
US20080254201A1 (en) * | 2004-10-22 | 2008-10-16 | Guya Bioscience S.R.L. | Method for Preparing Endosseous Implants with Zircon Dioxide Coating |
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US20190105427A1 (en) * | 2016-06-09 | 2019-04-11 | Michael Gahlert | Bone substitute material made of zirconium dioxide ceramic |
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