Abstract: A dental implant system includes an abutment including a first portion configured for disposal within an inner cavity of a dental implant and defining an outer surface configured for fixation with an inner surface of the dental implant. The abutment includes a second portion having a drive configured to separate from the abutment at a predetermined force. Methods of use are also disclosed.

Abstract: A gingival tissue retractor for retracting gingival tissue away from tooth and bone during a surgical procedure having an alveolar bone grip having an open frame structure positionable over at least one tooth and along a predetermined segment of an alveolar bone and providing an inward resilient force about opposite sides of the alveolar bone for maintaining position of the gingival retractor; a first gingival reflector having a solid plate structure and attached to a lower section of one side of the alveolar bone grip for providing a primarily downward force to gingival tissue on one side of the alveolar bone; and a second gingival reflector having a solid plate structure and attached to a lower section of another side of the alveolar bone grip for providing a primarily downward force to gingival tissue on another side of the alveolar bone.

Abstract: A system for delivering a surgical tack in tissue includes a driver, comprising: a shaft having a slot and a channel; and a handle slidably connected to said shaft and having a driving mechanism, said driving mechanism having a driving pin for providing a downward force through said shaft; and a tack cartridge having a plurality of tacks and adapted to be received in said slot and further adapted to feed said tacks between said driving mechanism and said channel.

Abstract: Compositions, methods and kits to be used as a lubricant and for treatment of a cavity pathology including joint pathology are provided. The composition comprises therapeutically effective amounts of at least one bioactive agent, such as magnesium compound, at least one lubricating agent, such as hyaluronic acid, and at least one cell membrane repairing agent, such as polyethylene glycol. The components of these compositions may be administered by a direct application, an application through a cannula, an intra-articular injection, as a flush fluid during an arthroscopy of the affected area, as a post-arthroscopy injection, or as part of a lavage of the area affected by the intra-articular pathology. In addition, the composition of the present invention may be administered to the patient from a pump or a depot.

Abstract: A chisel system for harvesting an implantable graft from an area of a human having a cartilage overlying a condyle, according to which a module is provided that has one end connected to a handle. A cutting surface is formed at the other end of the module that cuts through the cartilage and condyle.

Abstract: A bone scoring device having a body, a scoring member configured to engage a bone surface and a first biasing member connected to and configured to rotate the scoring member is provided. The scoring member being axially movable between a first, non-rotatable position, such that the scoring member is engaged with the body and a second rotatable position such that the scoring member is released from engagement with the body and freely rotates. The scoring member having an abrasive surface to score the surface of the bone in which it is put in contact. A method for using the scoring device as well as a kit including the scoring device are also provided.

Abstract: An implant includes a collar configured for disposal within tissue. The collar defines an axial bore. A shaft extends between a first end and a second end. The shaft is configured for disposal with the bore of the collar. A base defines an axial bore having an inner surface configured for engagement with the shaft such that the base is axially movable relative to the shaft. At least one arm extends between the collar and the base. The at least one arm is movable via axial movement of the base relative to the shaft between a first position and a second position such that the at least one arm is expanded in a configuration to engage tissue. Methods of use are also disclosed.

Abstract: A dental implant system includes bone growth promoting material configured for disposal within a body cavity about an implant. A protective element is configured to overlay the bone growth promoting material. Methods of use are also disclosed.

Abstract: The invention is directed to an adhesive strip, particularly an adhesive strip or bandage for use in periodontal treatments. The biocompatible adhesive strip comprises a flexible barrier with a biocompatible adhesive for use in an oral environment, wherein the adhesive is in a non-tacky state when dry and becomes adherent upon contact with liquids.

Abstract: Biodegradable stents and methods for selectively guided tissue regeneration in treating a periodontal defect adjacent to a root of a tooth are provided. The biodegradable stents and methods comprise a coronal portion and a transverse portion or shelf, which reduce unwanted migration of gingival epithelium, gingival connective tissue, and soft tissue and enable the cementum and periodontal ligament cells to re-establish the periodontal ligament in a proper sequence resulting in a new periodontal attachment.

Abstract: An implant includes an elongate body having at least two radially expandable portions in the vicinity of the distal end thereof. An expander is disposed at least partially within the axial bore of the body, the expander including a longitudinal shaft and a tip at the distal end of the shaft. The expander is longitudinally movable between a distal position wherein the tip is positioned distal to the distal end of the body and a proximal position wherein the expandable portions of the body are moved to a radially outward expanded configuration by a camming action of the tip.

Abstract: A surgical procedure for preparing a damaged area of a human knee to receive at least one graft according to which a moldable material is positioned over the damaged area and removed after it hardens. Cutting a tape in a configuration and dimension corresponding to the mold and forming at least one opening in the damaged area. Harvesting a graft from a biological sample that is configured to fit in the at least one opening, adhering the at least one graft to a surface of the tape and inserting the graft into each opening of the mold.

Abstract: A suture system that includes at least one suture having an end portion, a loop portion configured to be disposed about a fixed point and an anchor configured to be connected to the end portion for anchoring the suture to tissue adjacent to the fixed point, wherein the loop portion of the suture is disposed about the fixed point so as to reduce a gap between the tissue and the fixed point. A kit including at least one suture system, a surgical tool for manipulating the suture and written instructions of use are disclosed. A method for using the suture system is also described.

Abstract: An implant includes a body having an upper and lower ends, a longitudinal bore defined by a threaded interior surface, and a threaded exterior surface; at least one stabilizer arm associated with a corresponding longitudinal slot in the body, the stabilizer arm being hingedly attached to the body and having a bone gripping protuberance projecting laterally outward therefrom. The stabilizer arm is movable from a first position wherein the bone gripping protuberance is positioned within the bore and a second fully extended position wherein the bone gripping protuberance is positioned outside the threaded exterior surface of the body. The stabilizer arm is resiliently biased to the first position. A camming member is movable through the bore of the body from an initial position to a final position wherein the stabilizer arm is moved to the second stabilizer arm position.

Abstract: An implant includes a body having a longitudinal axis, at least one expandable portion configured to move between an unexpanded configuration and an expanded configuration, and at least one linearly and non-rotatably movable expander member configured to contact the at least one expandable portions such that linear movement of the expander member moves the expandable portion between the unexpanded configuration and the expanded configuration.

Abstract: Described are bone generation matrixes having an admixture of demineralized bone matrix (DBM) particles and/or bone chips in combination with at least one binding agent selected from the group consisting of alginate, lectin, pectin, gellan gum, starch, collagen and combinations thereof in an aqueous solvent, wherein the DBM particles and/or bone chips are present in an amount of at least 65% by dry weight and the ratio of the aqueous solvent to the dry weight of the DBM particles/bone chips and at least one binding agent is between about 1:1 to about 1:6.

Abstract: Compositions, methods and kits to be used as a lubricant and for treatment of a cavity pathology including joint pathology are provided. The composition comprises therapeutically effective amounts of at least one bioactive agent, such as magnesium compound, at least one lubricating agent, such as hyaluronic acid, and at least one cell membrane repairing agent, such as polyethylene glycol. The components of these compositions may be administered by a direct application, an application through a cannula, an intra-articular injection, as a flush fluid during an arthroscopy of the affected area, as a post-arthroscopy injection, or as part of a lavage of the area affected by the intra-articular pathology. In addition, the composition of the present invention may be administered to the patient from a pump or a depot.