Abstract: There is described a biocompatible implant for the filling of a cavity in a living organism such as, for example, a bone defect or an extraction wound, comprising an open porous scaffold and/or a composite matrix comprising a plurality of inorganic or synthetic granules and a synthetic polymer matrix, and further comprising a biodegradable membrane which is interconnectibly sealed to a surface portion of the scaffold or composite matrix such, that the scaffold or composite matrix and the membrane form a single piece of matter. In one embodiment, the implant is biodegradable.

Abstract: A method of fabricating an implant with improved surface properties and an implant fabricated using the same are provided. The method includes immersing a substrate that has titanium or titanium alloy in electrolytic solution including at least one of the group consisting of phosphate or fluoride ion and strontium ion, and forming an oxide film layer with a surface structure having a fine roughness of a micro scale by making at least one of phosphate or fluoride ion and strontium ion react to the titanium or the titanium alloy of the substrate on a surface of the immersed substrate using hydrothermal reaction associated with temperature, pressure and time conditions.

Abstract: Endosseous implant to be applied to a human or animal bone, wherein the surface of the implant is made from titanium or a titanium alloy, said implant having a smooth or rough surface texture, which is characterized in that said surface has been treated with at least one selected organic phosphonate compound or a pharmaceutically acceptable salt or ester or an amide thereof; process for producing said implants.

Abstract: The present invention refers to a system of prosthetic components consisting of Compensatory Slanted Copings and Abutments of Universal Coupling that function as a set of coupled parts that allow corrections of slants that vary between OQ and 60Q, of fixing osseointeg rated implants, including zygomatic fixations, and it provides a cap, molding transferer and screws for fastening and locking. This system of copings and abutments provides properties of conversion and extension of the implants. Its shape provides better occlusal stability and favorable biomechanics, since the forces are better distributed, diminishing the concentration of tension on the fitting platform of the implant, as well as the screws. The abutments of the universal coupling can be readjusted and be cemented or screwed. In the present system, the superior platform of the coping and the inferior base of the abutment are universalized, since the inferior platform of the coping corrects the slant of the implant.

Abstract: Exemplary embodiments relate to a dental abutment and methods of forming the same. The abutment (19) may include a head portion (27) located at an upper end of the abutment and constructed to support a prosthetic tooth replacement and soft tissue adjacent the head portion, an anti-rotation feature (25) located at a lower end of the abutment and constructed to mate with a dental implant, and a fillet (21) located at an interface between the head portion and the anti-rotation feature. The fillet may reduce a risk of fracture at the interface between the head portion and the anti-rotation feature. In some examples, the abutment may be formed at least partially of a ceramic material.

Abstract: The invention relates to a method for producing a functional prosthesis as a provision for a jaw region, allowing for the procedural steps of taking a dental impression of the jaw region to be provided with the functional prosthesis, producing a preliminary structure and possibly testing the preliminary structure in an articulator, and producing the functional prosthesis on the basis of the possibly re-worked preliminary structure.

Abstract: The curved plate is used to position and model a malleable material capable of temporarily supporting the incisor and pinless teeth according to positions and orientations that will then be fixed permanently in the prosthesis. The plate has a general U shape, delimited by two parabola-shaped contours: an outer edge and an inner edge, respectively corresponding to the contour of the vestibular walls of the incisor and pinless teeth of the prosthesis to be built. The plate features a flat surface on its lower face, and an appendix defining a visible reference point that must correspond to the position of the interincisive papilla. The distance between the reference point and an average central point of the outer edge indicating a position situated between the more vestibular walls of the upper central incisor teeth, is between 8 and 10 mm.

Abstract: An attachment system for removably securing a dental superstructure to a dental implant is provided. This attachment system has a first part, connected to, or arranged at, said dental superstructure, and a second part, connected to, or arranged at, said dental implant. These parts are removably securable to each other. An attachment device and an anchoring element that may be comprised in such a system are also provided.

Abstract: The invention provides a method for dental restoration including direct modification of an abutment in the oral environment to obtain the ideal shape, contour, and margin placement. The method is featured with directly measuring the shortest distance X1 between a location L1 on the surface of the abutment and the surface of a surrounding object, and increasing the shortest distance X1 until it is not less than a predetermined value. The invention exhibits numerous merits such as simplified procedure, cost-effectiveness, reduction of laboratory adjustment, reduction of chair time, and reduction of office visits.

Abstract: A fixing member for an implant which comprises a tube or a pillar made of an hydroxyapatite ceramics at least one part of which is a ceramics porous article consisting essentially of a hydroxyapatite formed by agitation foaming, in which a number of approximately spherical pores mutually contact having pore structures communicated three-dimensionally opened at the contact area and having an averaged porosity of from 65% to 85%. A method for fixing an implant comprising a step of inserting an implant whose at least one part of the periphery is integrated with a hydroxyapatite ceramics into an implant insertion site of an alveolar bone or a gnathic bone. A method for fixing an implant, a fixing member for the implant and an implant composite in order to reinforce an implant insertion site by compensating or regenerating an alveolar bone or a gnathic bone on an implant treatment in dentistry or in oral surgery is obtained.

Abstract: A temporary supraconstruction for a dental implant or a core for a temporary supraconstruction for a dental implant, characterized in that it includes a material having a modulus of elasticity of less than 300 MPa, preferably in the range of from 15 to 20 MPa.

Abstract: The subject matter of the invention is, in one example, a dental implant for implantation in a human or animal jawbone with an implant for receiving a dental prosthesis. Providing a dental implant that can be implanted with less discomfort for the patient is achieved in that the implant is at least in parts surrounded with bone substance of the patient, said bone substance not originating from the place in the jaw of the patient at which the dental implant is intended to be implanted.

Abstract: Disclosed is a kit useful in connection with the preparation of dental prostheses and including an implant-abutment analogue and a burnout coping. The analogue generally corresponds to an implant and abutment in the jaw of a patient. A burnout coping is secured to the analogue for the preparation of the dental prosthetic. In one embodiment, the analogue includes a connection feature and the coping includes a mating connection feature, the connection feature on the coping positioned to provide a remnant on the dental prosthetic prepared thereform that does not interfere with the placement of the prosthetic onto an implant and abutment in the jaw of a patient. In another embodiment, not mutually exclusive with respect to the first embodiment, the coping comprises first and second portions that are movable with respect to one another and sized respectively to engage first and second portions of an analogue.

Abstract: The invention discloses a novel implant provided with a macroporous surface on the top surface, and a method for the production of such a metallic and/or ceramic implant having a textured, particularly porous, surface for the at least partial insertion in hard tissue, such as in a bone, and/or into soft tissue. The implant is produced as a green compact, at least in sections, using a cold isostatic pressing, casting, and/or injecting (CIM, MIM) with subsequent sintering to obtain an implant, and is particularly characterized in that the surface is modified and/or prepared before sintering such that a macroporous surface is present after sintering without requiring any finishing.

Abstract: The invention relates to the examination of a dental prosthesis, wherein the dental prosthesis is examined with finite element methods. Furthermore, the invention relates to the automated manufacture of a dental prosthesis, wherein the shape of a remaining tooth area is directly determined on the basis of the remaining tooth area itself. Furthermore, the invention relates to a method, wherein manufacturing data (milling data) which have been created with a system for calculating manufacturing data (system for calculating milling data) are optionally forwarded to one or another manufacturing machine (milling machine) at different locations.

Abstract: A dental prosthetic substructure comprising an alloy. In one embodiment, the alloy comprises a first mixture comprising about 50 percent to about 99.95 percent by weight of the alloy and a second mixture comprising at least 0.05 percent to about 5 percent by weight of the alloy. The first mixture comprises at least two precious metals. The second mixture comprises at least one precious metal.

Abstract: One-part dental implant (5) with an anchoring part (10) for anchoring in the bone and with a build-on part (15) for receiving an element to be applied. The build-on part has at least one core (25) and a covering layer (30) which are visually and/or acoustically different from one another.

Abstract: A method for manufacturing a multipart assembly of sintered oxide ceramic material, including one first component which at least partially surrounds one second component in such a manner that detaching the first component from the second component is not possible without destroying the first and/or second component. The assembly is produced by producing a single-part first shaped part and a single-part second shaped part from an oxide ceramic blank, whereby the first shaped part and the second shaped part are enlarged to compensate for the shrinkage during sintering, and assembling the sintered shaped part as second component with the first shaped part and subsequently sintering them together.

Abstract: A method for producing a dental prosthesis, including obtaining data for the teeth that are to be replaced and for their surrounding area; compiling a database containing data for prefabricated tooth replacement parts; excluding those tooth replacement parts which, based on the data recorded for the teeth to be replaced and for their surrounding area, are unsuitable for functional and/or aesthetic and/or stability reasons; selecting the tooth replacement parts to be used; using imaging software to obtain a virtual representation of the tooth replacement parts integrated into the surrounding area in the patient's dentition in accordance with customary set-up rules; recording the data of an actual situation in a patient's mouth after preparation of the affected teeth and insertion of any implants; checking the compliance of the selected tooth replacement parts with the data of the actual situation after preparation; making available the selected tooth replacement parts; modifying the selected tooth replacement

Abstract: The invention concerns a method for the production of a dental product, whereby the impression of a negative mold of at least one tooth or one tooth stump is created with an impression material, and this negative mold is scanned. By using the scan results, the dental product is then mechanically produced.

Abstract: In the process for producing dental prostheses such as bridges, crowns implants, etc. from ceramic material, production is carried out at least by way of one CAD/CAM machining station. The ceramic material to be worked consists of an unsintered disk-shaped blank or one which has not been subjected to final sintering, working of the blank into dental prostheses being undertaken at a right angle or quasi-right angle to the parallel or quasi-parallel surfaces of the blank.

Abstract: Dental articles are produced using relatively low sintering temperatures to achieve high density dental articles exhibiting strengths equal to and greater than about 700 MPa. Ceramic powders comprised of nanoparticulate crystallites are used to manufacture dental articles. The ceramic powders may include sintering agents, binders and other similar additives to aid in the processing of the ceramic powder into a dental article. The ceramic powders may be processed into dental articles using various methods including, but not limited to, injection molding, gel-casting, slip casting, or electroforming, hand, cad/camming and other various rapid prototyping methods. The ceramic powder may be formed into a suspension, pellet, feedstock material or a pre-sintered blank prior to forming into the dental article.

Abstract: A material for dentures having a 3-point bending strength of at least 1300 MPa, dentures produced from said type of material, corresponding blank materials, a method for producing blanks, and a method for producing a denture part made from said material or a blank.

Abstract: The present invention provides polymeric substrates comprising a biocompatible coating and methods of preparation thereof. In particular, the coating may be a ceramic material, especially a calcium phosphate material, which may be functionally graded. The invention provides the ability to apply high quality coatings to polymeric substrates without damaging the substrate (e.g., melting the polymeric material). The functionally graded coating can provide crystalline calcium phosphate near the coating interface with the substrate and provide amorphous calcium phosphate at the outer surface of the coating.

Abstract: An implant which includes a shaft made of a first material and having an exterior surface, and at least one thread made of a second material different from the first material, engaging the exterior surface, and extending outwardly from the exterior surface for engaging bone. After implantation of the implant, bone tissue may osseointegrate into the porous shaft to anchor the implant within the surrounding bone. The first material may be a porous metal and include tantalum while the second material is non-porous.

Abstract: A dental implant is provided having an anchoring part for anchoring the dental implant in the bone and an abutment for fastening a superstructure, the abutment being connected to the anchoring part, and the anchoring part and the abutment being based on zirconium oxide. The anchoring part is provided with at least two substantially cylindrical bodies, the center axes of which extend in the same direction and which are integrally connected to one another at upper ends, so as to form the abutment, and which can be inserted into corresponding holes in the jaw bone.

Abstract: An implant includes a head portion, an intermediate portion and an initially separate stem portion configured to engage the head portion so that at least the head portion and the stem portion cooperatively secure the intermediate portion on the implant. The implant may also include a locking mechanism configured to secure the head portion to the stem portion by a press fit or a threaded connection. The intermediate portion may include a porous metal such as tantalum.

Abstract: Method according to which an individual implant (19) is modelled taking into account the individual shape of a tooth (2) and/or a hole (6) in a jaw-bone (3).

Abstract: The invention relates to a method for producing tooth prosthesis parts comprising an implant for inserting into the jaw and a prosthesis for securing to an implant by means of a connecting surface (52). A first measuring data set of a 3D X-ray image is prepared in the region of the prosthesis which is to be inserted and is reproduced on a display unit (1) as a 3D X-ray model (20). A second measuring data set of a three-dimensional optical measurement of the visible surface of the jaw and of parts of the adjacent tooth (11, 12) is prepared in the region of the prosthesis which is to be inserted. The measuring data set of the 3D X-ray image is correlated with the measuring data set of the three-dimensional optical measurement in relation to the geometries. A data set of the prosthesis is prepared as a 3D prosthesis model (40). The 3D prosthesis model (40) is displayed to-scale in the correlated 3D X-ray model (20) on the display unit (1).

Abstract: A material comprising: from 98-50% by volume of zirconia as a matrix, which is stabilized with i) either of from about 2 to about 3 mole percent of yttria ii) or of from about 10 to about 15 mole percent of ceria; iii) or a mixture of ceria and yttria in the range of amounts as given in i) and ii) the stabilizing oxides may be substituted against each other in a ratio from 1:99 to 99:1 and a maximum stabilization of 3 mole percent related to pure yttria and 15 mole percent related to pure ceria respectively are not exceeded, and wherein the term mole percent is related to the zirconia matrix and wherein the zirconia matrix is obtainable from a) a powder of particles of zirconia having a mean particle size of <0.

Abstract: An implant according to the invention includes first thermoplastic material portions, and second thermoplastic material portions liquefiable by mechanical vibrations and being in contact with the first thermoplastic material portions, wherein the second thermoplastic material portions preferably constitute at least a part of a surface of the implant, and wherein the first thermoplastic material portions have a glass transition temperature above an implantation temperature (about 20° C. to 40° C.), and wherein the second thermoplastic material portions either have a glass transition temperature below said implantation temperature or include means for transforming non-mechanical energy into heat.

Abstract: Provided are implants having a porous coating, comprising an implant core made of solid material and a sleeve fitted thereon, wherein the sleeve comprises an outer porous region in addition to an inner non-porous region. The invention further provides a method for joining the solid implant core and a sleeve comprising an outer porous region as well as an inner non-porous region.

Abstract: The invention relates to a method for producing a powder-filled ceramic coating made from a precursor ceramic compound (for example, a sol-gel), said coating having an advantageous surface roughness and wherein active ingredients may be eluted from the matrix or filler under physiological conditions and to an implant which can be produced according to the claimed method.

Abstract: Compositions and methods are provided for a cosmetic dental structure, comprising a veneer body sized to cover at least a portion of a tooth structure. The veneer body has a front face and a reinforcement rib extending outwardly from a rear face of the veneer body. The reinforcement rib can be configured to strengthen the veneer body, and the reinforcement rib and veneer body are configured to be adhered to the tooth structure.

Abstract: A manufacturing method and dental component are provided in which first and second cast parts are used with a casting material, such as a gel slurry, to form the dental component. The first cast part can be positioned in a space of the second cast part and a gel slurry can be applied intermediate the first and second cast parts. The gel slurry can then be solidified to form a solidified gel slurry. The first cast part can then be removed together with the solidified gel slurry from the second cast part. The solidified gel slurry can then be machined to form an exterior shape corresponding to a desired exterior shape of the dental component. Finally, the solidified gel slurry can be sintered.

Abstract: A method for determining a sintering shrinkage of a pre-sintered body. The method includes providing a green preform with at least one design feature. The green-preform is pre-sintered to form a white body. At least one change in the at least one design feature with the pre-sintering is recorded. An expected sintering shrinkage to a dense-sintered component is determined using the recorded change.

Abstract: A manual driver for a dental implant drill or other dental implant tools and the method of use for preparing for dental implantation are provided. The manual driver includes a handle, an extension shank and a chuck having an axial channel configured to receive and interlock an implant drill, and a fastening screw transverse to the axial channel. The method of manual preparation for dental implantation using the manual driver has a high precision, and reduces the risk of bone cracking caused by vibration of motor-driven drilling. The manual drilling method provides better tactile sensation and drilling control to the dentist. Further, the method avoids drilling irrigation, allows collection of virgin bone tissue from the drills, and reintroduces the collected bone tissue in the receiving bore to promote bone regeneration after the implantation.

Abstract: The invention relates to the examination of a dental prosthesis, wherein the dental prosthesis is examined with finite element methods. Furthermore, the invention relates to the automated manufacture of a dental prosthesis, wherein the shape of a remaining tooth area is directly determined on the basis of the remaining tooth area itself. Furthermore, the invention relates to a method, wherein manufacturing data (milling data) which have been created with a system for calculating manufacturing data (system for calculating milling data) are optionally forwarded to one or another manufacturing machine (milling machine) at different locations.

Abstract: The invention relates to a process for the production of a dental prosthetic item (10) by means of local sintering, in which the dental prosthetic item (10) is produced layer-wise by energy input, by means of an energy transferring beam (7), into a layer of powder (6) of a sinterable material. One or more parameters of the sintering process are modified during production such that the material (6) is regionally sintered to various degrees to produce denser material in the marginal region (14) of a sintered layer of said dental prosthetic item (10) than is produced in the inner region (15) of said sintered layer. The invention furthermore relates to a dental prosthetic item (10) of a material subjected to local sintering, which material is sintered in a marginal region (14) of the dental prosthetic item (10) to a greater density than in an inner region (15).

Abstract: The present invention relates to a method for obtaining an accurate three-dimensional model of a dental impression, said method comprising the steps of, scanning at least a part of an upper jaw impression and/or a lower jaw impression, obtaining an impression scan, evaluating the quality of the impression scan, and use the impression scan to obtain a three-dimensional model, thereby obtaining an accurate three-dimensional model of the dental impression.

Abstract: The invention relates to a process, a blank, an assortment of blanks, a tooth database, and a database of blanks, for the production of a dental prosthetic item. The method comprises the provision of a 3D model of a dental prosthetic item and the selection of a suitable blank from a plurality of possible blanks. The provision of the 3D model of the dental prosthetic item comprises the determination of an esthetically relevant designed subregion of the 3D model of the dental prosthetic item as part of an exterior surface of said dental prosthetic item, and a blank is specified from a plurality of blanks having a prefabricated esthetically relevant terminal subsurface of a surface of the tooth, the terminal subsurface of said blank being such that it at least approximates the thus specified designed subregion. The 3D model of said dental prosthetic item is carved from the selected blank such that the prefabricated terminal subsurface of said blank remains unmachined in at least a central region thereof.

Abstract: The present invention relates to an artificial implant or a part thereof coated with at least two drugs, a method of preparing the same and a method of treating a subject, wherein the implant according to the invention is implanted into a subject.

Abstract: The present invention relates to a dental implant having recombinant bone morphogenic protein coated on the processed surface thereof, which, when implanted into the jawbone, enables undifferentiated adult cells around the implant site to be rapidly differentiated into osteoblasts so as to induce osteoconductive healing to thereby reduce a healing period, as well as a coating method thereof. According to the invention, recombinant bone morphogenic protein BMP-2 penetrates between ceramic balls formed on the dental implant surface, sheet structures of calcium triphosphate or fine pores formed by anodic oxidation, so as to form a coating film. Thus, the recombinant bone morphogenic protein BMP-2 is not detached from the dental implant surface even during the surgical implantation of the implant.

Abstract: The present invention relates to a treatment method of the implant abutment surface to increase adhesion between the implant and its surrounding soft tissue, to prevent epithelial down-growth, to prevent bacterial infection, and to extend life-time of the implant and an implant surface-treated by the same. The method for treating surface of the dental implant or implant abutment is characterized by microgroove-formation having greater width and bottom width than the section diameter of a human gingival fibroblast and by additional acid-etching on the whole surface including ridges which used to be left as polished, so that filopodia is actively stretched out to increase adhesion between the implant and its surrounding soft tissues.

Abstract: A therapeutic compound, methods and applicators to prevent and treat focal tissular lesions and infections in mammals is made by the mixture of an antiseptic powder and an antiseptic liquid, wherein the compound may be employed for an “assisted integration” through the “bone socket arrangement” pre or post-implantation by medication in a patient, for preventing or curing by direct contact diseases within the mouth and also to treat skin inflammations, infections, aphthas, herpes simplex infections, ulcers, burns, and other externally illness, to promote healing and bone growth and to chemical debridement.

Abstract: This invention relates to ink-jet printing systems for making dental products such as artificial teeth, dentures, splints, veneers, inlays, onlays, copings, frame patterns, crowns and bridges and the like. An ink-jet printer is used to discharge wax-like polymerizable material in a layer-by-layer manner to build-up the object. In other methods, a heated capillary or dropper can be used to apply the polymerizable material. The resulting three-dimensional object has good dimensional stability. Light irradiation can be used to cure and harden the material, thereby producing the final dental product.

Abstract: Dental appliances including multiple components and a system and method for constructing the same are disclosed herein. The dental components are designed to fit together to form the dental appliance. The components of the dental appliance are electronically modeled, printed, and pressed sequentially, separately, or as a unitary piece. Forming the dental appliance from multiple components enables each component of the dental appliance to be formed from a different material, each material having different features associated with it. In various embodiments, different materials have different colors, textures, opacities, and transformation factors associated with them. Furthermore, each component can be formed from multiple components. In some other embodiments, a support structure is designed and constructed in order to minimize deformation of a dental component during fabrication of the component.

Abstract: An improved cosmetic accessory device for teeth that simulates the appearance of an assemblage of teeth and gum. The device includes a gum portion and a tooth portion shaped and dimensioned to cover the user's upper or lower front teeth. The device is made of a nontoxic, nonirritating, tasteless, odorless, resilient, easily cleaned and chemically stable material that does not stick to natural teeth, gums, or most dental work. In use, the device is held in place by custom-fitted inner projections that match the spaces between the user's own front teeth. Optionally, a shelf extending just across the front teeth and extra fitting material placed in spaces where there are missing teeth provides additional security in holding the device in place. The device may be refitted as necessary by simply partially submerging the device in hot water.

Abstract: Muffle (1) for the production of dental prostheses (2), said muffle (1) being a body that is substantially rotationally symmetrical about the muffle axis (A), characterized in that the proportion of cylindrical surface regions (31) about the muffle axis (A)—relative to the total surface area of the outer contour (3) of the muffle (1)—is less than 30%, preferably less than 20%.

Abstract: An implant, in particular an implant for dental applications, is provided at least partially in the area of its surface with a protective layer. The protective layer is intended to avoid the deposition of contaminants. The protective layer is chosen such that it breaks up on contact with body fluids and/or bone, with the result that essentially no residues remain on the surface of the implant.