86 results about "Implant supported" patented technology

The invention relates to a method and device for placing implants (1) using a surgical template (11) which is made from tomographic cuts in the patient's jawbone (7). According to the invention, step drills (4) and calibrating drills (5), having a single standard diameter for each type of implant (1), are guided through drill bushings (18) which are inserted into bores (15) in the template (11) in order to produce any drilling sequence corresponding to an implant plan. The penetration depth of the drills (4, 5) is controlled by the height of the bores (15) or by the drill rings (21). The aforementioned template (11) bores (15) serve as a guide for the precise placement of the implants (1) owing to the adapted implant supports (3). Moreover, washers (23), which are mounted around the implant supports (3), limit compression in relation to the implants (1) while said implants are being placed (20). The above-mentioned characteristics serve to limit the required number of drills (4, 5) and implant supports (3) to the longest models only. The inventive method and device are particularly suitable for computer-assisted implantology systems.

The invention relates to a method and device for placing implants using a surgical template which is made from tomographic cuts in the patient's jawbone. Step drills and calibrating drills, having a single standard diameter for each type of implant, are guided through drill bushings which are inserted into bores in the template in order to produce any drilling sequence corresponding to an implant plan. The penetration depth of the drills is controlled by the height of the bores or by the drill rings. The method limits the required number of drills and implant supports to the longest models only. The inventive method and device are particularly suitable for computer-assisted implantology systems.

A breast implant has at least an outer shell which is composed of a resorbable material. The implant, which can be formed entirely of bioresorbable material such as a collagen foam, is sized and shaped to replace excised tissue. The implant supports surrounding tissue upon implantation, while allowing for in-growth of fibrous tissue to replace the implant. According to various alternative embodiments, the implant is elastically compressible, or can be formed from self-expanding foam or sponges, and can be implanted through a cannula or by injection, as well as by open procedures. The implant can carry therapeutic and diagnostic substances.

An instrument for preparing a surface of a joint is provided. The glenoid surface is adapted for receiving a prosthetic component having a feature closely conforming to the surface. The prosthetic component provides a bearing surface for a head portion of a long bone. The instrument includes a guide having a first feature and a second feature and a tool. The tool is used for cooperation with the first feature for preparing the surface. The first feature is adapted to at least partially control the position of the tool as it prepares the surface. The second feature is adapted to assist in positioning of the guide with respect to the joint.

The invention relates to a method and device for placing implants (1) using a surgical template (11) which is made from tomographic cuts in the patient's jawbone (7). According to the invention, step drills (4) and calibrating drills (5), having a single standard diameter for each type of implant (1), are guided through drill bushings (18) which are inserted into bores (15) in the template (11) in order to produce any drilling sequence corresponding to an implant plan. The penetration depth of the drills (4, 5) is controlled by the height of the bores (15) or by the drill rings (21). The aforementioned template (11) bores (15) serve as a guide for the precise placement of the implants (1) owing to the adapted implant supports (3). Moreover, washers (23), which are mounted around the implant supports (3), limit compression in relation to the implants (1) while said implants are being placed (20). The above-mentioned characteristics serve to limit the required number of drills (4, 5) and implant supports (3) to the longest models only. The inventive method and device are particularly suitable for computer-assisted implantology systems.

In one aspect, a group of inter-connecting, prefabricated components of various shapes and sizes that can be assembled together to form a framework system directly onto dental implants installed in the patient's mouth is disclosed. In another aspect, a group of prefabricated components to form a drill guide system for drilling a properly spaced and oriented implant hole adjacent to another implant hole or adjacent to a fully-installed implant is disclosed. In yet another aspect, improved procedures for installing permanent, implant-supported dental restorations are disclosed, including an immediate loading procedure.

A tissue marking implant includes a matrix material and a dye marker. The implant, which can be formed entirely of bioresorbable material such as a collagen foam, is sized and shaped to replace excised tissue. The implant supports surrounding tissue upon implantation, while allowing for in-growth of fibrous tissue to replace the implant. According to various alternative embodiments, the implant is elastically compressible, or can be formed from self-expanding foam or sponges, and can be implanted through a cannula or by injection, as well as by open procedures. The implant can carry therapeutic and diagnostic substances. The dye marker leaches from the implant such that a surgeon, upon subsequent surgical intervention, visibly recognizes the tissue marked by the dye marker.

Provided are fibrous composites prepared by methods of the present invention, comprising oxides and biodegradable polymers, in which the fibers are made of aerogel-like oxide materials having nanometer-sized pores. The fibrous composition advantageously has, at least, the following characteristics: (i) a very high nanoporous surface area, which also permits nucleation of crystallites; (ii) mesoporous / macroporous interspacial networks between the fibers, providing high bioactivity and a high transport rate; (iii) macropores for natural one-like tissue growth; (iv) good mechanical properties for handling and for implant support; and (v) biodegradability for implant dissolution and time-variable mechanical properties. Further provided are methods for using the bioactive biodegradable fibrous composites as osteogenic composite materials for tissue engineering, tissue re-growth, bone implants, and bone repair, and / or for the delivery of drugs or therapeutic compounds.

In one aspect, a group of inter-connecting, prefabricated components of various shapes and sizes that can be assembled together to form a framework system directly onto dental implants installed in the patient's mouth is disclosed. In another aspect, a group of prefabricated components to form a drill guide system for drilling a properly spaced and oriented implant hole adjacent to another implant hole or adjacent to a fully-installed implant is disclosed. In yet another aspect, improved procedures for installing permanent, implant-supported dental restorations are disclosed, including an immediate loading procedure.

An instrument for preparing a surface of a joint is provided. The glenoid surface is adapted for receiving a prosthetic component having a feature closely conforming to the surface. The prosthetic component provides a bearing surface for a head portion of a long bone. The instrument includes a guide having a first feature and a second feature and a tool. The tool is used for cooperation with the first feature for preparing the surface. The first feature is adapted to at least partially control the position of the tool as it prepares the surface. The second feature is adapted to assist in positioning of the guide with respect to the joint.

Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and / or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy / breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast.

A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone.

An improved system and method for the design, creation and installation of implant-supported dental prostheses is provided. A network accessible portal facilitates communication among a dental professional, a scanning center, a manufacturing center and others in the design and production of a dental drill guide and prosthesis, utilizing cone beam imaging, a rotatable 3-dimension representation of a patient's jaw, virtual placement of one or more implants and virtual testing prior to manufacture. Dental professionals may access the portal on a subscription or non-subscription basis.

Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and / or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy / breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast.

A pelvic implant assembly having a support member and an insertion tool. The insertion tool having an implant support portion for supporting the support member as it is being inserted into a tight therapeutic location within a patient. The support member is coupled to and extends between the implant support portions prior to insertion into the incision. Once the insertion tool and accompanied support member are in the therapeutic location the insertion tool can open and spread out the support member. The insertion tool can also dilate the tissue as it opens, thereby, eliminating the need to dissect tissue.

Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and / or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the ingrowth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy / breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast

Absorbable implants for breast surgery that conform to the breast parenchyma and surrounding chest wall have been developed. These implants support newly lifted breast parenchyma, and / or a breast implant. The implants have mechanical properties sufficient to support a reconstructed breast, and allow the in-growth of tissue into the implant as it degrades. The implants have a strength retention profile allowing the support of the breast to be transitioned from the implant to regenerated host tissue, without significant loss of support. Three-dimensional implants for use in minimally invasive mastopexy / breast reconstruction procedures are also described, that confer shape to a patient's breast. These implants are self-reinforced, can be temporarily deformed, implanted in a suitably dissected tissue plane, and resume their preformed three-dimensional shape. The implants are preferably made from poly-4-hydroxybutyrate (P4HB) and copolymers thereof. The implants have suture pullout strengths that can resist the mechanical loads exerted on the reconstructed breast.

A urethral occlusive assembly includes an implant component and external component. The implant component includes a flexible bridge member connecting two opposed implant supports. The implant component is implanted about a dorsal surface of an animal urethra. An external component is disposed external to and proximate the animal urethra. The external component operatively communicates with the implant component to transmit a compressive load on the urethra. By communication between the implant and external components, either the implant component or the external component actively compresses the urethra against the flexible bridge member, thereby effecting urinary continence.

A tissue marking implant includes a matrix material and a dye marker. The implant, which can be formed entirely of bioresorbable material such as a collagen foam, is sized and shaped to replace excised tissue. The implant supports surrounding tissue upon implantation, while allowing for in-growth of fibrous tissue to replace the implant. According to various alternative embodiments, the implant is elastically compressible, or can be formed from self-expanding foam or sponges, and can be implanted through a cannula or by injection, as well as by open procedures. The implant can carry therapeutic and diagnostic substances. The dye marker leaches from the implant such that a surgeon, upon subsequent surgical intervention, visibly recognizes the tissue marked by the dye marker.

An improved system and method for the design, creation and installation of implant-supported dental prostheses is provided. A network accessible portal facilitates communication among a dental professional, a scanning center, a manufacturing center and others in the design and production of a dental drill guide and prosthesis, utilizing cone beam imaging, a rotatable 3-dimension representation of a patient's jaw, virtual placement of one or more implants and virtual testing prior to manufacture. Dental professionals may access the portal on a subscription or non-subscription basis.

A spinal implant includes a first component including a first surface configured for engagement with a first vertebral surface and a second surface configured to define at least a portion of an implant support cavity. A second component is connected to the first component and includes a first surface configured for engagement with a second vertebral surface and a second surface configured to define at least a portion of the implant support cavity. A removable intermediate component is configured for disposal in the implant support cavity. The intermediate component is inflatable to move the first component relative to the second component to expand the interbody implant from a first configuration to a second, expanded configuration. At least one agent is configured to replace the intermediate component in the implant support cavity in the second configuration. Methods of use are disclosed.

A spinal implant includes a first component including a first surface configured for engagement with a first vertebral surface and a second surface configured to define at least a portion of an implant support cavity. A second component is connected to the first component and includes a first surface configured for engagement with a second vertebral surface and a second surface configured to define at least a portion of the implant support cavity. A removable intermediate component is configured for disposal in the implant support cavity. The intermediate component is inflatable to move the first component relative to the second component to expand the interbody implant from a first configuration to a second, expanded configuration. At least one agent is configured to replace the intermediate component in the implant support cavity in the second configuration. Methods of use are disclosed.

A tissue marking implant includes a matrix material and a dye marker. The implant, which can be formed entirely of bioresorbable material such as a collagen foam, is sized and shaped to replace excised tissue. The implant supports surrounding tissue upon implantation, while allowing for in-growth of fibrous tissue to replace the implant. According to various alternative embodiments, the implant is elastically compressible, or can be formed from self-expanding foam or sponges, and can be implanted through a cannula or by injection, as well as by open procedures. The implant can carry therapeutic and diagnostic substances. The dye marker leaches from the implant such that a surgeon, upon subsequent surgical intervention, visibly recognizes the tissue marked by the dye marker.

A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone. A method for treating a bone comprising: selecting at least one reinforcing element to be combined with an injectable matrix material to form a composite implant capable of supporting the bone; positioning the at least one reinforcing element in a cavity in the bone; flowing the injectable matrix material into the cavity wherein the injectable matrix material interfaces with the at least one reinforcing element; and transforming the injectable matrix material from a flowable state to a nonflowable state to establish a static structure that supports the adjacent bone.

The invention belongs to the technical field of dental restoration, and discloses a dental chair-side implant restoration digitization implementation method. The method comprises the following steps: scanning and acquiring internal formation of the mouth cavity of a patient by adopting in-mouth scanning equipment to realize data acquisition; transmitting the acquired data into a dental restoration system; forming a three-dimensional mouth cavity model capable of being subjected to edition processing and restoration design in the dental restoration system based on the acquired data to further carry out data matching between an implant database and the acquired data in the dental restoration system; forming an analog image of the implant in the mouth of the patient in the three-dimensional mouth cavity model at the same time; carrying out restoration design of a personalized base and a dental crown of the patient on the formed three-dimensional mouth cavity model to form an implant-supported prosthesis; transmitting the data of the formed implant-supported prosthesis into processing equipment to realize formation of the implant-supported prosthesis; processing the formed implant-supported prosthesis and directly bringing into the mouth of the patient to realize implant restoration in the mouth of the patient. The dental chair-side implant restoration digitization implementation method is suitable for being applied to the field of dental restoration.

A fixed, implant-supported, full arch dental prosthetic having a dental prosthetic body, a rigid fence and a gingival veneer. The dental prosthetic body is prefabricated from a cured dental resin, and the rigid fence and the gingival veneer are respectively constructed from a curable dental resin. The dental prosthetic body, which can be included in a dental kit, may be prefabricated in various shapes and sizes and with various tooth forms. The dental kit also contains a supply of at least one curable dental resin, such as for constructing the rigid fence and / or the gingival veneer of the dental prosthetic and / or for affixing the dental prosthetic to an array of dental implants embedded in a patient's mouth.

A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone.

An intervertebral implant that can be surgically introduced between adjacent vertebrae and expanded in situ to occupy an optimal space between the vertebrae. The implant is inserted into the evacuated disc space obliquely and then oriented so as to extend laterally across the anterior adjacent vertebrae with its outer ends of the implant supported by the cortical rims on the opposite sides of the vertebrae. The implant has two body members with a space therebetween so the implant may be then distracted and a spacer of predetermined thickness that may be inserted within the space between the body members so as to maintain a desired amount of distraction. The upper and lower surfaces of the implant may have a desired lordotic angle. A method of using an implant is disclosed which permits endoscopic visualization of the disc space.

A composite implant comprising an injectable matrix material which is flowable and settable, and at least one reinforcing element for integration with the injectable matrix material, the at least one reinforcing element adding sufficient strength to the injectable matrix material such that when the composite implant is disposed in a cavity in a bone, the composite implant supports the bone. A method for treating a bone comprising: selecting at least one reinforcing element to be combined with an injectable matrix material to form a composite implant capable of supporting the bone; positioning the at least one reinforcing element in a cavity in the bone; flowing the injectable matrix material into the cavity wherein the injectable matrix material interfaces with the at least one reinforcing element; and transforming the injectable matrix material from a flowable state to a nonflowable state to establish a static structure that supports the adjacent bone.

A direct clamp robotic finishing system is provided including a robot, a gripper secured to the robot, and a pair of fingers secured to the gripper. A tray assembly is also provided for supporting a plurality of implants for picking up by the fingers. An implant reorientation station is provided for supporting the implant being maneuvered by the robot as the robot re-grips the implant from a new direction. The fingers directly clamp the implant thereby eliminating the need for dedicated implant support bars.