EP1796575A1 - Implant de dent individuelle intra-osseux presentant une meilleure capacite d'integration tissulaire - Google Patents
Implant de dent individuelle intra-osseux presentant une meilleure capacite d'integration tissulaireInfo
- Publication number
- EP1796575A1 EP1796575A1 EP05767490A EP05767490A EP1796575A1 EP 1796575 A1 EP1796575 A1 EP 1796575A1 EP 05767490 A EP05767490 A EP 05767490A EP 05767490 A EP05767490 A EP 05767490A EP 1796575 A1 EP1796575 A1 EP 1796575A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- base body
- implant
- end edge
- implant according
- tooth implant
- 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.)
- Withdrawn
Links
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
- 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
- A61C8/0012—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
- A61C8/0048—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
-
- 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
- A61C8/0054—Connecting devices for joining an upper structure with an implant member, e.g. spacers having a cylindrical implant connecting part
-
- 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
- A61C8/0018—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
- A61C8/0018—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
-
- 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
- A61C8/0059—Connecting devices for joining an upper structure with an implant member, e.g. spacers with additional friction enhancing 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
- A61C8/0068—Connecting devices for joining an upper structure with an implant member, e.g. spacers with an additional screw
-
- 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
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
-
- 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
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
- A61F2002/30838—Microstructures
-
- 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
- A61F2/30767—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
- A61F2/30771—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
- A61F2002/3085—Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with a threaded, e.g. self-tapping, bone-engaging surface, e.g. external surface
- A61F2002/30858—Threads interrupted by grooves or sidewalls, e.g. flat sidewalls
-
- 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
- A61F2310/00—Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
- A61F2310/00389—The prosthesis being coated or covered with a particular material
- A61F2310/00976—Coating or prosthesis-covering structure made of proteins or of polypeptides, e.g. of bone morphogenic proteins BMP or of transforming growth factors TGF
Definitions
- the invention relates to an intraosseous single-tooth implant for a fixed dental prosthesis, with a substantially cylindrical or slightly conical, in a recess present in a Kieferkno ⁇ Chen or inserted into a jaw bone insertable body having a blind hole open to its coronal end , an essentially hollow-cylindrical implant structure, which can be attached to the cranial end edge of the base body and which has an apical centering collar which opens into a hollow-cylindrical annular recess of the base body which is open towards the coronal end of the base body.
- the implant assembly can be used pers, at least at its coronal end open bore for receiving a directly into the blind bore of the body or indirectly insertable and implant assembly at least partially penetrating implant abutment screw and a substantially on the longitudinal center axis of the annular recess radial shoulder support surface of the body can be placed , radial shoulder substantially to the longitudinal central axis of the Implantat inconveniencehalte ⁇ , wherein the annular recess is formed near the cranial end edge of the body as a substantially hollow cylindrical guide sleeve for wesentli chen cylindrical guide collar of the implant structure, whoseêt notebook ⁇ diameter substantially matching the inner diameter the guide sleeve coincides, and in the region of the guide sleeve and the guide collar of the main body on the one hand and of the implant abutment on the other hand complementary complementary fit are provided for non-rotatably connecting the implant assembly and the base body, and a mounting head for the dentures.
- this object is achieved in that the outer diameter of the guide collar of the implant structure is smaller than the outer diameter of Grundkör ⁇ pers in the region of its cranial end edge; that a coronal substantially exposed end edge surface is formed between a peripheral Stimrandkante of the body and an inner end edge edge thereof; that the shoulder support surface of the main body projects inwardly within the annular recess radially inward from the inner wall of the annular recess; and that the outer wall of the base body, at least in the region of the guide sleeve, is roughened up to the peripheral end edge of the base body and / or is microstructured and / or nanostructured.
- the front edge surface of the body roughened and / or micro- and / or nanostructured.
- the entire outer surface of the base body is roughened and / or microstructured and / or nanostructured.
- the outer peripheral surface of the implant structure is roughened and / or microstructured and / or nanostructured at least in its region which adjoins the end edge surface of the base body after insertion into the basic body.
- An embodiment of the invention provides that the outer circumferential surface of the implant structure is roughened and / or microstructured and / or nanostructured at least in a region which, after insertion of the implant structure into the basic body, is approximately 1-2 mm extends from the end edge surface of the main body. It can also be provided according to the invention that the entire outer surface of the implant structure extends, after insertion of the implant structure into the main body, crannially from the end edge surface to a shoulder of the implant abutment on which a crown of the dental prosthesis is seated.
- the invention optionally proposes that the shoulder support surface of the Grundkör ⁇ pers axially closer to the end edge of the body than the interlocking elements ("anti-rotation elements").
- the invention can also provide that the shoulder support surface of the main body of Stirn ⁇ edge of the body axially further away than the interlocking elements.
- the surface normal of the end edge surface lies at all circumferential points of the end face of the stimulus in a plane parallel to the longitudinal central axis of the main body and of the implant abutment.
- the axial distance from the end edge of the main body to the shoulder support surface thereof varies from about 0.1 to about 3 mm.
- the invention optionally proposes that the axial distance from the end edge of the body circularly to the shoulder support surface thereof is about 0.1 to 3mm.
- the outside surface roughness depth of the base body and / or of the implant structure has a microstructure size of less than 10 ⁇ m and / or is nanostructured It can be provided that the outer surface roughness depth of the base body and / or the implant structure is about 5 microns.
- the outer surface roughness in the nano range already alone optimizes the hydrophilicity of the surface (ultrahydrophilia) and thus promotes better tissue attachment. It also serves to condition the surface for covalent or noncovalent binding of tissue growth factors.
- the roughened and / or microstructured and / or nanostructured surface of the base body and / or the implant structure may be prepared, at least in regions, preferably chemically for covalent and / or non-covalent bonding with a biologically active substance and / or with a biologically active substance biologically active substance is coated.
- the biologically active substance may be covalently and / or non-covalently bound, as proposed in WO 99/26674.
- the implant surface can also be chemically prepared, as also described in WO 99/26674, in order to bind active substances which are either physiologically present in the prepared implant bed or additionally introduced into the borehole in a suitable administration form with the implant the implant can be applied before implantation.
- a particular embodiment of the invention provides that the biologically active substance has one or more bone growth factor (s).
- the biologically active substance has one or more connective tissue factor (s).
- the biologically active substance will have one or more mucous membrane growth factor (s).
- a further embodiment of the invention provides that the biologically active substance has one or more blood vessel growth factor (s).
- these biologically active substances may thus be bone-inductive, connective tissue-inductive, blood-vessel-inductive and / or mucosal-inductive.
- the invention is based on the surprising finding that it is possible by means of a combination of features according to the invention to obtain the intimate bone implant connection, once formed during the healing phase (closed, transgingival or / and transperiosteal), in its vertical height level in a stable manner and qualitatively To improve (possibly also later possibly otherwise resulting bacterially induced "peri-implantitis" phenomena to prevent) that in combination the front edge surface of the body is exposed and thus there is a bone-bordering connective tissue attachment (An ⁇ storage) as "covering adhering" arises and at the same time in the interior of the body or its annular recess displaced axial support of the shoulder of the implant assembly on the shoulder support surface of the body for a erhebli ⁇ che improvement in the "rigidity" of the connection between the body and implant structure leads.
- Bone ⁇ storage bone-bordering connective tissue attachment
- the connective tissue adhering to the end edge and on the end edge surface causes the bone to be distanced from the epithelial attachment (mucosal attachment) as part of the biological "width.”
- it also acts as "shock absorption" against micromovements that inevitably occur can occur in extreme conditions even with virtually rigid connections between the implant base and Implantatauf ⁇ construction and thereby give rise to mechanically induced inflammatory phenomena and initiate bone resorption, even without additional bacterial influence at the top of the body.
- the epithelial attachment (mucosal attachment) is formed on the implant structure that protrudes cranially from the implant body.
- the apical portion of the implant structure which extends into the annular recess of the implant body and extends cranially to the crown shoulder of the implant structure, may also be completely or partially microstructured and / or nanostructured.
- the implant structure at the apical portion of which the hemidesmosomal attach ⁇ ment of the connecting epithelium (mucosal attachment) is also repeatedly removed without causing vertical bone resorption (adaptation).
- the junction (hem) ephithelium adheres at the interface to the connective tissue via hemidesmosomes and therefore remains largely intact.
- the implant is placed transgingivally (not covered / on time) and the implant structure is inserted directly, then the epithelial attachment forms above the end edge surface, and the connective tissue attachment separating from the bone can develop during the healing phase and develop its immunological defense competence.
- the implant abutment has to be removed again at a later time in order to prevent others Temporarily screwing system components in and out can be done without unwanted bone resorption / adaptation.
- Figure 1 shows an embodiment of the invention in a partially sectioned longitudinal view
- the endosseous single-tooth implant according to the invention in the embodiment shown there on a provided with external thread 10 body 12, with its lying in the drawing below apical end first in a left by a tooth extraction in the jawbone of a patient recess or a in the jaw bone appropriately introduced hole can be screwed.
- Basic body of this kind are basically known from DE 40 28 855 and / or from DE 195 34 979 C1, to which reference is made to supplement the description in this respect.
- the base body 12 which is designed to be closed at its apical end shown in FIG. 1, has a blind bore open towards its coronal end lying in the drawing above.
- an implant assembly 14 in the prior art according to DE 40 28 855 Cl and DE 195 34 979 Cl therminologically called “spacer sleeve" used, which is formed substantially hollow and in which a not shown in the Zeich ⁇ tion Implant abutment screw (referred to in the aforementioned state of the art as "implant post”) can be inserted from the coronally open end, which passes through the likewise apically open end of the implant assembly 14 and in an internal thread 16 near the apical end of an annular recess 18, forms substantially hollow cylindrical worked ⁇ , the base body 12 is used, wherein the aforementioned annular recess 18 extends from a coronal end edge 20 of the base body 12 to the apical, lying in the drawing below end of the internal thread 16.
- the implant assembly 14 By screwing the implant assembly retaining screw into a substantially hollow cylindrical, apically and coronally open bore 22 of the implant assembly 14 and screwing the implant assembly retaining screw into the internal thread 16, the implant assembly 14 becomes fixed and in a maximum manner relative to the base body 12 non-relatively movable in the base body 12 held.
- the end edge 20 of the main body 12 has a peripheral end edge 24 and an inner end edge of stimulation 26, through the mutual distance of a substantially perpendicular to a longitudinal central axis 28 of the base body 12 and thus the implant assembly 14 ver ⁇ running end edge surface 30 is formed. This is achieved in that the outer diameter of the implant abutment 14 in its region adjacent to the end edge 20 after insertion is smaller than the outer diameter of the main body in the region of the end edge 20.
- the end edge surface 30 by no means necessarily has along its entire circumference the longitudinal central axis 28 of the main body constant distance from the api ⁇ cal end of the base body 12, but can with respect to the longitudinal extent of Base body 12 be up and down, whereby an optimal adaptation of the "axia ⁇ len" contour of the end edge surface 26 of the natural shape of the jaw bone, in which the base body 12 is to be used, is achieved. In this way, it is possible to achieve that the end edge surface 30 is substantially flush with the surface of the jawbone or, depending on the needs and wishes of the treating physician, at a certain distance below or above the surface of the jawbone in the region of the implant insert can be arranged.
- the desired course of the end edge surface can be adapted intraoperatively to the bone conditions individually with a suitable device.
- the implant assembly 14 has a guide collar 32, which engages in a subsequent to the end edge 20 of the body 12 guide sleeve 34 fits.
- a radially extending shoulder 36 which extends substantially perpendicularly to the longitudinal center axis 28 of the base body 12 and the implant assembly 14, is provided which adjoins an apically arranged complementary shoulder support surface 38 of the base body 12 Insert is present.
- FIG. 2 also shows complementary interlocking elements 40 of both the main body 12 and the implant abutment 14, which engage in one another, for example from DE 195 34 979 C1, and after insertion of the implant abutment 14 into the main body 12, a twisting of the implant abutment 14 prevent the main body 12 about the longitudinal central axis 28.
- These interlocking elements 40 may, for example, in the form of mutually complementary grooves and projections in the base body 12 on the one hand and the implant assembly 14 be trained on the other hand, but here omitted a more detailed drawings Darstel ⁇ description and description, rather in this regard, to supplement the description, for example, to DE 195 34 979 Cl is pointed out.
- the substantially cylindrical peripheral outer surface of the guide sleeve 34 and the end edge surface 30 of the base body 12 are in the embodiment shown micro and / or nanostrucured, namely. by chemical etching or laser treatment.
- the roughness extends in the embodiment shown, moreover, over the entire outer surface of the base body 12, although restrictions on the roughening on insbe ⁇ special the cylindrical outer surface of the guide sleeve 34, with simultaneous roughening or roughening of the end edge surface 30, are possible.
- the measures described on the one hand ensures that the implant assembly 14 as a result of the displacement of the "" stop "between the shoulder 36 of the implant assembly 14 and the shoulder support surface of the body 38 in the interior of the annular recess 18 a particularly rigid connection between the body 12th and the implant assembly 14 is ensured.
- This in combination with the roughening of the outer surface of the base body 12 in the region of the guide sleeve 34 and the end edge surface 30, ensures that the jawbone in the substantially cylindrical to slightly conical portion of 34 enters into an intimate connection with the base body 12 and the resting Connective tissue in an optimal manner intimately connects with the outer surface of the base body 12 in the region of the frontal edge surface 30. This intimate connection of bone and connective tissue also remains stable in function.
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dentistry (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Prostheses (AREA)
Abstract
La présente invention concerne un implant de dent individuelle intra-osseux pour une prothèse dentaire fixe avec une structure d'implant et un corps de base. Le diamètre extérieur de la nervure de guidage de la structure d'implant est inférieur au diamètre extérieur du corps de base dans la zone de son bord frontal crânien. Une surface de bord frontal coronaire sensiblement dégagée est formée entre une arête de bord frontale périphérique du corps de base et une arête de bord frontal interne de celui-ci. La surface d'appui d'épaulement du corps de base dans la cavité annulaire fait saillie vers l'intérieur de manière principalement radiale depuis la paroi interne de la cavité annulaire. La paroi externe du corps de base est rugueuse et/ou microstructurée et/ou nanostructurée au moins dans la zone du manchon de guidage jusqu'à l'arête de bord frontal périphérique du corps de base.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE200410043317 DE102004043317A1 (de) | 2004-09-08 | 2004-09-08 | Enossales Einzelzahnimplantat mit verbesserter Gewebeintegrationsfähigkeit |
DE102004063893A DE102004063893A1 (de) | 2004-09-08 | 2004-09-29 | Enossales Einzelzahnimplantat mit verbesserter Gewebeintegrationsfähigkeit |
DE102005001792A DE102005001792A1 (de) | 2005-01-13 | 2005-01-13 | Enossales Einzelzahnimplantat mit verbesserter Gewebeintegrationsfähigkeit |
PCT/DE2005/001221 WO2006026938A1 (fr) | 2004-09-08 | 2005-07-12 | Implant de dent individuelle intra-osseux presentant une meilleure capacite d'integration tissulaire |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1796575A1 true EP1796575A1 (fr) | 2007-06-20 |
Family
ID=38038953
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05767490A Withdrawn EP1796575A1 (fr) | 2004-09-08 | 2005-07-12 | Implant de dent individuelle intra-osseux presentant une meilleure capacite d'integration tissulaire |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP1796575A1 (fr) |
WO (1) | WO2006026938A1 (fr) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012011834A1 (fr) * | 2010-07-20 | 2012-01-26 | Vasiliev Vladimir Alexeevich | Implant dentaire et variante |
BR102014031426B1 (pt) | 2014-12-15 | 2018-07-24 | Jjgc Ind E Comercio De Materiais Dentarios S/A | implante |
USD816841S1 (en) | 2014-12-15 | 2018-05-01 | Jjgc Industria E Comercio De Materiais Dentarios S/A | Bone implant |
BR102016010184B1 (pt) | 2016-05-05 | 2020-10-27 | Jjgc Indústria E Comércio De Materiais Dentários S.A. | conjunto protético e processo para produção do mesmo |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR7202932D0 (pt) * | 1972-02-24 | 1973-12-06 | H Brainin | Implante dental |
FR2213760B1 (fr) * | 1973-01-12 | 1976-05-14 | Portoukalian Jean Marie | |
US6214049B1 (en) * | 1999-01-14 | 2001-04-10 | Comfort Biomedical, Inc. | Method and apparatus for augmentating osteointegration of prosthetic implant devices |
JP2003518980A (ja) * | 2000-01-04 | 2003-06-17 | シュトラウマン・ホールディング・アクチェンゲゼルシャフト | 骨内の歯科インプラントおよび組み合わせ構造体 |
WO2002000133A1 (fr) * | 2000-06-28 | 2002-01-03 | Albert Zickmann | Implant dentaire |
WO2003030767A1 (fr) * | 2001-10-11 | 2003-04-17 | Dentium Co., Ltd | Dispositif de fixation et de montage conçus pour une operation d'implantation |
DE50305740D1 (de) * | 2003-01-23 | 2007-01-04 | Dinkelacker Wolfgang | Knochenimplantat und Verfahren zu seiner Herstellung |
-
2005
- 2005-07-12 WO PCT/DE2005/001221 patent/WO2006026938A1/fr active Application Filing
- 2005-07-12 EP EP05767490A patent/EP1796575A1/fr not_active Withdrawn
Non-Patent Citations (1)
Title |
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See references of WO2006026938A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO2006026938A1 (fr) | 2006-03-16 |
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