Abstract: Disclosed is a device and method for use in the dental implant industry. Generally, the device relates to packaging systems for dental implants that are capable of storing implants of different lengths and varying diameters. An embodiment of the package may be composed of a vial for housing a cushion. Located on the cushion is a sleeve for housing at least a portion of a dental implant. The sleeve and implant are covered by a sleeve cap whereby the sleeve cap is constructed to hold a healing screw. The packaging system also includes a lid for covering the healing screw.

Abstract: An implant (10) has one or more surfaces (10a, 10b) with a basic or starting surface structure (1a) derived from mechanical working. A topographic modification of the surface structures is arranged on said surface structure or surface structures. The topographic modification can be formed, for example, by means of shot-peening, etching, plasma spraying, chemical action, etc. The topographically modified surface structures support bone-growth-stimulating agent. In a method for producing the implant, three subsidiary methods are used for carrying out the mechanical working, the topographical modification, and the application of the bone-growth-stimulating agent. An important niche in the demand which exists in the field of implants is thus covered in an advantageous manner.

Abstract: The stability of an implant (5) which is fitted in a jaw bone hole created by tooth root extraction is increased using osteoinductive material. Bone formation in the space between the implant and the bone wall is also stimulated. In an initial stage, the implant is anchored or fitted in the hole. With its outer parts (5a) the implant extends into a part (4a) of the hole which has a cross-sectional area exceeding the cross-sectional area of the outer parts (5a) of the implant. The soft tissue of the jaw bone, with possible periosteum, covers the implant and the space to form a closed space (4a). The bioactive material consists of growth-stimulating substances (GSS) arranged on the implant In a stage of incorporation, GSS passes outward into body fluid which has penetrated into the closed space and interacts with cells present in the fluid so that new bone is formed around the outer parts (5a) of the implant. The invention also relates to a use and to an implant.

Abstract: In an arrangement with implant and attachment part/dental bridge, the latter comprises one or more recessed walls. The implant is designed or can cooperate with a portion which can be arranged on a spacer sleeve belonging to the implant and extends substantially parallel to the recessed wall. The attachment part and its respective recessed wall is arranged with displaceability in the main longitudinal direction of the implant relative to the outer surface of the portion. The portion is arranged to be expandable so that, in a given position of longitudinal displacement, it is possible to achieve interaction between outer surfaces of the portion and the recessed wall and thus anchoring of the attachment part to the portion or the implant. The invention also relates to a device with two or more implants and dental bridge. By means of the invention, discrepancies between dental bridge and the implants can be taken up in an effective and rapid securing principle.

Abstract: The invention relates to a method for treating an implant, and to an implant treated by said method. All or some of the outer surfaces of the implant are oxidized with a layer (1a) of substantial thickness and substantial porosity or pore volume. One or more CaP layers (12) are applied to the porous surface or surface of large pore volume. Bone-growth-stimulating agents (13), for example rh-BMP-2 or rh-BMP-7, are then applied to the CaP layer. The method and the device make it possible to support a maximum quantity of bone-growth-stimulating agent, which can be controlled in respect of its release function.

Abstract: In connection with implants for bone or tissue, delivery of bioactive substances to the bone or tissue is ensured. The implant is designed with an internal space, and one or more bodies comprising the bioactive substance are designed to cooperate with the bone and/or tissue structure surrounding the implant and to release the bioactive substance to the said structure. The said body or bodies is/are applied in the space in order thereby to be exposed to the surrounding structure and deliver the bioactive substrate or substances to the latter.

Abstract: A system useful in producing a three-dimensional body comprising bone or tissue-compatible material includes a detection and analysis site which identifies and simulates a portion of a body in connection with an implantation situation. A production device produces a model responsive to the simulation information. A flame-spraying apparatus provides the bone-compatible and/or tissue-compatible material in a powder form through a nozzle. Relative movement between the nozzle and a support member supporting the model or die is controlled to apply one or more layers of the bone-compatible material to the model. A method includes using a computer to identify and simulate a body in connection with a given implantation situation, and producing a model or die accordingly the bone or tissue-compatible material is flame-sprayed in a powder form. Movements of a nozzle and/or a supporting member are controlled so as to effect a desired surface characteristic on the three-dimensional body.

Abstract: An arrangement for producing a blank made of metal powder, preferably titanium powder, intended for a dental crown or other product for the human body (spacer, dentine, implant, etc.) comprises at least one first apparatus for powder compression and at least one second apparatus with one or more elastic molds having at least one cavity for a punch (block) and the powder used in the initial stage. The first apparatus comprises a machine operating by impact compaction, and said mold or molds is/are arranged, when the cavity is filled with starting powder, to receive impacts effected by the impaction members in the machine and, as a function of the impact or impacts, to generate an isostatic action during the compression/compaction. The invention also relates to a device, method and use and permits a rapid production procedure while maintaining the current requirements in respect of precision and quality.

Abstract: A device, for example in the form of an implant, is arranged to be applied via at least one surface or one portion (for example an outer portion) to bone and/or tissue in the human body. An agent which stimulates bone growth, in the form of HA, is used in connection with the device. The device, the surface or the portion comprises or consists of compressed bone-compatible and/or tissue-compatible material in the form of titanium powder. The titanium powder is mixed with the agent, which is also in powder form, and a composite material is formed with the two powders by means of impact compaction. The invention also relates to a method and use in connection with devices of the type in question. A novel type of HA use is made possible and eliminates, inter alia, the disadvantages of loosening HA layers during production of the device.

Abstract: A superstructure is included together with other components in a tooth prosthesis system, by means of which a tooth prosthesis is intended to be applied to a patient in a short application time, for example in one or only a few days. The superstructure (1) is designed with a bearing part (1b) which can cooperate with fixture members, and a tooth-prosthesis-supporting part, and the parts are designed with recesses for said securing members. The bearing part and the tooth-prosthesis-supporting part are integrated over at least most of their horizontal extents by means of the parts being produced from a common blank or a material composition using a treatment or method which gives a user-friendly outer shape and bevels on the unit or superstructure forming the parts.

Abstract: A self-tapping implant for jawbone comprises a body (15) with threads arranged thereon, a conically tapering portion (12) arranged at its front end, and one or more spaces (4, 5, 6) which accommodate bone material cut off during tapping and which are formed by removal of material from the threads and body in question. Each materially reduced thread has a cutting edge (1a, 2a, 3a) which extends inwards from the outer edge of the respective remaining thread part and which can cooperate with the bone during tapping. Each cutting edge of a number of cutting edges has a pointed shape (1b, 2b, 3b) which, in the cross section of the thread in question, essentially follows a line which deviates from a radius (r) through the remaining thread part's front portion or the pointed shape's point (1b, 2b, 3b) in order in this way to form a cutting angle. Each cutting edge (1a, 2a, 3a) on a first remaining thread part (1, 2, 3) merges via a radius (r?) or curved part into a rear edge (e.g.

Abstract: A method for producing a model for an oral prosthesis in the human body. A model top part and a model bottom part are selected having oblique assembly surfaces. The model bottom part includes an outer surface that slopes outwards from a bottom surface of the model bottom part. The outer surfaces of different bottom model parts have different maximal heights. The model bottom part and the model top part are arranged in a mutual rotational position in dependence upon a vertical extent of the oral prosthesis in relation to a securement in the bone. The model top part and the model bottom part are put together and anchored to one another by their assembly surfaces. Malleable material is applied to at least a top part of the assembled model top part and bottom part, thereby realizing an outer surface of the oral prosthesis.

Abstract: An arrangement including a spacer element operative to support a superstructure and including a first passage and a second passage. The second passage is operative to permit mechanical anchoring of the holder. A first screw is operative to screw the spacer element into an implant. During an initial stage of insertion the first passage is operative to receive the first screw such that a center axis of the first screw is inclined in relation to a direction of screwing of the first screw. During a final stage of insertion the first passage permits the first screw to tilt such that the center axis of the first screw substantially coincides with the direction of screwing. A holder is operative to hold the spacer element. The holder substantially prevents the first screw from leaving the position it has assumed during the final stage of insertion. A second screw is operative to screw the superstructure onto the spacer element.

Abstract: A self-tapping implant for use in a jawbone includes a body with plural thread spirals arranged thereon; a conically tapering portion arranged at a front end of the body and having one or more bone-chip recesses therein which accommodate bone material cut off during a tapping operation. The bone-chip recesses are formed by removal of material from the plural thread spirals and body. At least in the conically tapering portion, the plural thread spirals are materially reduced, and each of the materially reduced threads have a cutting edge which extends inward from an outer edge of a respective remaining thread part. Each cutting edge of a number of associated cutting edges of the materially reduced threads have a pointed shape which, in a cross section thereof, essentially follows a line which deviates from a first radius through a point of the pointed shape of the respective remaining thread part.

Abstract: An apparatus includes a template which locates hole positions in a jawbone while the template is separated from the jawbone by gum tissue. The template follows a contour of the gum tissue surrounding the jawbone and has guide holes which receive a cutting tool. Anchoring elements attach the template to the jawbone. A system includes means for scanning an implantation site on a patient's jawbone, simulating the implantation site, and determining nerve-rich areas or nerve paths in the jawbone. A holed template is produced which is separated from the jawbone by at least gum tissue of the patient. Attachment hole positions in the jawbone are located so as to avoid nerve paths. A method of forming holes to attach a dental implant to a patient's jaw bone without surgical intervention in gum tissue of the patient to expose the jawbone is disclosed which avoids impingement on a nerve path.

Abstract: A method for securing a spacer to an implant integrated in bone. A spacer and a screw are engaged with a holder in a rotationally fixed position with respect to the holder. The spacer is engaged in a spacer engaging portion of the holder and the screw is engaged in a screw engaging portion of the holder. The screw is inserted in a threaded receiving passage of the implant such that threads on the screw engage threads of the receiving passage. A rotational motion is applied to the holder, thereby rotating the rotationally fixed spacer and screw and screwing the screw into the receiving passage of the implant. A cooperation between a bearing surface of the spacer and a top surface of the implant is established at a predetermined position of screwing. The holder is separated from the spacer and the screw.

Abstract: An operating site is used to assemble individually designed dental products, for example spacers, abutments, bridges, etc. Each product consists of two or more structural elements. The operating site is provided with computer equipment which can reproduce a simulated model of the jaw, jawbone, implant, etc., and structural elements applied to the model. The operating site is arranged to collate data in a profile relating to part of the assembly. Members are included for transmitting profile data via the network to the central unit. The central unit supplies information relating to the part in question. The information is sent to the operating site or to a production unit connected to the central unit for production of the part. A debiting system is arranged to indicate to the central unit or to the production site that the information or production, respectively, has been paid for.

Abstract: An impression cap for taking dental impressions in a patient's mouth comprises a distal end that includes a top surface and a proximal end that defines an opening. The impression cap also includes an inner surface that defines an internal cavity. The proximal end of the impression cap is configured to engage a corresponding shoulder of a prosthetic abutment in a snap fit. The impression cap further comprises an injection port configured to receive a tip of an injection syringe for injecting impression material under into the inner cavity and a plurality vent holes configured to allow air and excess impression material to escape from the inner cavity. Methods of using the impression cap and a dental kit including the impression cap are also disclosed.

Abstract: An implant for application in bone, especially jaw bone, is provided. The implant includes a unit that can be applied in the bone, and which is made of a biocompatible material such as titanium. The unit is provided with one or more coatings including calcium phosphate and a bone-growth-stimulating substance that initiates and/or stimulates bone growth. The coating is applied at least to surface parts of the unit cooperating with the bone. A method of producing the implant is also provided.

Abstract: A prosthodontic assembly comprises a restoration having a cavity defined by a first surface and an abutment positioned within the cavity. The assembly further comprises a plurality of standoffs positioned in between the first surface and the abutment to provide a gap. Methods for forming the restoration are also disclosed.