Abstract: The invention relates to a scan abutment (2), in particular an integrally manufactured scan abutment, for determination of the position of the front face (1.1) of a dental endosseous implant (1), wherein the abutment (2) has a longish, hollow shaft (4), and the shaft has an upper region (4.1), a central region (4.2) and a lower region (4.3). Moreover, the shaft (4) of the scan abutment with its central region (4.2) is attachable onto the front face (1.1) of the implant (1), and its lower region (4.3) is insertable into the connection geometry of the implant. The longish, hollow shaft (4) has a side wall (10). The shaft of the scan abutment has at least two to terminally extending slits (5) in its central region (4.2) and lower region (4.3) in the side wall (10). Two, three or four slits are preferred. Preferably, the slits (5) end in one recess (6) each, such as a circular recess, in the side wall (10) at their upper end and extend terminally in the side wall (10) to the bottom side of the shaft (4).

Abstract: A dental implant is described and includes a threaded coronal portion having a top hollow part with a cavity and an opening in a top portion of the hollow part, wherein the top hollow part is defined by sacrificial walls of the coronal portion, wherein a width of the cavity and the opening allows insertion of a cutting element of a dental saw into the cavity.

Abstract: Dental implants for fixed and removable prosthetic devices, having application to single tooth replacement, e.g., caps and crowns, and multiple tooth replacement using one or more implants, e.g., bridges, and multiple implants for full and partial prosthetic devices. Dental implants include an implant and an abutment configured to mate with the implant in a non-rotatable fashion. The implant may have a cylindrical or a non-cylindrical shape. In one embodiment, the dental implant includes a first stage implant and a second stage implant. The second stage implant is interconnectable to the first stage implant and includes an abutment with an anatomical emergence profile. Further, dental reconstruction and abutment installation methods utilizing the dental implant systems and instruments are disclosed. Also provided are impression taking procedures, and impression copings that produce an accurate fit between the dental prosthesis and the dental implant.

Abstract: The present invention relates to an integrated hybrid dental implant, and more particularly, to an integrated hybrid dental implant in which an opening portion formed at a screw body to enable a drug to be injected into an implantation site of the implant, and the mechanical stability is excellent despite the presence of the opening portion. The integrated hybrid dental implant according to the present invention enables a drug to be supplied to the area around the implantation site so as to induce bone regeneration into the implant after the implant has been placed at a bone-deficient site, has an additional mechanical strength when bone grows into the side openings and hollow inner channel, and allows the screw body to be integrally formed with the prosthesis section (i.e., one piece) to exhibit more excellent mechanical strength so that the implant can be useful as a dental implant.

Abstract: An automotive intraoral scanner applied in a mouth includes a biting piece, a track piece and at least one mobile image processing set. The biting piece is sandwiched between two rows of teeth. The track piece is installed in the biting piece and disposed corresponding to the rows of teeth, and a shape of the track piece is similar to a shape of the rows of teeth. The mobile image processing set is installed on the track piece and moved along the track piece, and the mobile image processing set is disposed corresponding to the rows of teeth. Therefore, the automotive intraoral scanner has advantages of easy operation.

Abstract: A system and method for creating a model of a patient's mandible and any teeth supported from the mandible and manipulating the mandible relative to anatomical features of the patient's maxilla. The system uses markers positioned on the mandible and on the maxilla to create a functional mandibular axis that approximates an axis through the condyles of the patient. The functional mandibular axis and geometric and anatomical information about the patient's upper and lower jaw are then used to create prostheses for the patient. The system is also used for making corrections to the prosthesis.

Abstract: The invention relates to a method for producing a dental prosthesis having the following chronological method steps: a) a first, provisional dental prosthesis comprising at least one first prosthetic base (1) and several provisional prosthetic teeth (4) is produced, whereby data that indicate at least the 3-dimensional form of the occlusal surfaces (6) of the provisional prosthetic teeth (4) of the provisional dental prosthesis are stored as data record A or have already been stored as data record A b) after subtractive occlusal processing of at least one of the provisional prosthetic teeth (4), at least the 3-dimensional occlusal surfaces (6) of the processed provisional prosthetic teeth (4) of the first dental prosthesis are determined, or the 3-dimensional surface of the first dental prosthesis is determined as a whole c) data that indicate at least the 3-dimensional form of the occlusal surfaces (6) of the processed provisional prosthetic teeth (4) are stored as data record B d) via a computer comparison

Abstract: A prosthodontic device applicable to the remainder of a root of a tooth that has received complete endodontic therapy includes a post and a core integrally formed with one end of the post. The post has a post body and a connection unit formed on the surface of the post body. The core has a head to sit on the top end of the remainder of the root of the tooth and at least one shoulder formed on the head. The largest diameter of the core is larger than the largest diameter of the post body of the post. The prosthodontic device enables rapid completion of tooth preservation and restoration after endodontic therapy.

Abstract: The present invention provides for oral care systems comprising: an appliance comprising a first and second plurality of nozzles, the appliance configured to be held in the mouth of a user with the first and second plurality of nozzles in fluid communication with one or more surfaces of the user's oral cavity; a source of gas; a source of liquid; and a fluid controller for directing entrained fluid to the appliance. Also provided are methods of cleaning, or otherwise providing oral care benefits to, one or more surfaces of the oral cavity using a system of the present invention.

Abstract: The present invention provides for oral care systems comprising: an appliance comprising a first and second plurality of nozzles, the appliance configured to be held in the mouth of a user with the first and second plurality of nozzles in fluid communication with one or more surfaces of the user's oral cavity; a source of gas; a source of liquid; and a fluid controller for directing entrained fluid to the appliance. Also provided are methods of cleaning, or otherwise providing benefits to, one or more surfaces of the oral cavity using a system of the present invention.

Abstract: An injecting gun for the treatment of animals with identification aid with a push button on the handle comprising a body formed by two main housings linked by their edges with delimitate the free space, in which there is an electronic card consisting of: a CPU (Central Processing Unit) which is connected by means of: a) UART (Universal Asynchronous Receiver/Transmitter) modules with: i) a RFID UHF module, and ii) a Bluetooth module; b) GPIO (General Purpose input/Output) modules with: iii) a plurality of LEDs (Light Emitting Diode), iv) a vibrator, vi) a buzzer vii) a syringe sensor, viii) two touch switches, and ix) a TFT (Thin-Film Transistor) liquid crystal parallel port; c) a USB module (Universal Serial Bus) with: x) a micro USB plug (micro USB); wherein, said CPU is connected to a memory; and wherein said CPU is connected to an energy source, which is connected to a charger and energy manager.

Abstract: An injecting gun with driven built-in counter, having a loading tube with a support for a needle at its distal end and a sliding plunger attached to a rod with transversal slots ending in a handle; a trigger associated with a cam that, when triggered, pushes the rod through the slots where said cam is settled, and a body including therein an electronic card constituted by a CPU connected to: a) GPIO modules connected with: i) a plurality of tactile switches, ii) a balance switch, iii) a OLED display, iv) a keyboard with associated LEDs, v) a buzzer, and vi) a speaker; y b) a USB module connected with: vii) a micro USB plug; wherein, said CPU is linked to a memory; tactile switches are associated to the trigger; and an energy source with energy manager is connected to said CPU and modules providing the energy needed for functioning.

Abstract: Sphincter reinforcement devices are described. Sphincter reinforcement devices may be configured to be placed at least partially around a bodily passage at or near a sphincter. In one embodiment, a sphincter reinforcement device may comprise a ring including a tubular structure. The ring may be expandable. The tubular structure may be hollow. The tubular structure may have a first end and a second end. The first end may be configured to be coupled to the second end. The tubular structure may include a braided material.

Abstract: Implantable artificial bronchi for the treatment of chronic obstructive pulmonary diseases, such as pulmonary emphysema. The implantable artificial bronchus can be made with silicone or nitinol. The embodiments of this invention may be further associated with a one-way valve.

Abstract: A prosthetic assembly for repairing a target tissue defect within a target vessel region configured includes an exclusion structure sized to substantially bypass target tissue defect, and includes a branch assembly. The branch assembly can include a self-expanding outer branch prosthesis having an inflow region configured to deform to a non-circular cross-sectional-shape when deployed, and a support structure at least partially disposed within the inflow region. The support structure preserves blood flow to the branch vessel while the deformed inflow region inhibits blood leakage between and/or around the prosthetic assembly.

Abstract: An adjustable construct for fixation of a tendon or ligament graft in a tunnel. The construct comprises a flexible, adjustable loop connected to tissue (for example, graft, ligament or tendon). The adjustable loop may be integrated with an additional tissue supporting device (for example, a wedge or a plug). The tissue is secured within a bone socket/tunnel by adjusting the length of the flexible adjustable loop.

Abstract: The present application relates to devices and methods for harvesting a skin graft(s) and introducing one or more nucleic acid, one or more amino acid sequences, or a combination thereof into one or more cells of the skin graft. The present invention provides transfecting the skin graft to modulate a cellular response that enhances epithelialization and/or pigmentation.

Abstract: An implant includes a hollow biocompatible shell, first and second electrodes, filling material, and circuitry. The hollow biocompatible shell is configured to be implanted in an organ of a patient. The first electrode is disposed inside the shell. The second electrode has at least one surface disposed outside the shell. The filling material, which includes carbon nanotubes (CNT), fills the shell and is configured, in response to a rupture occurring in the shell, to change a spatial orientation of the CNT and thus to cause a change in electrical conductivity of the filling material between the first electrode and the rupture. The circuitry is electrically connected to the first and second electrodes and is configured to detect the rupture by sensing the change in the electrical conductivity of the CNT, and to produce an output indicative of the detected rupture.

Abstract: Corneal transplant procedures may involve suturing an implant of healthy corneal tissue to a recipient cornea. The sutures may cause unwanted deformation of the corneal implant and the recipient cornea. A supporting structure may be embedded into the corneal implant to enhance the stability of the corneal implant and the recipient cornea and to reduce the likelihood of unwanted deformation when the corneal implant is sutured to the recipient cornea. According to one embodiment, a corneal implant includes donor corneal tissue extracted from a donor cornea. The donor corneal tissue includes an interior channel formed at a depth below an anterior surface. The corneal implant includes a supporting structure formed from non-tissue material and positioned in the channel.

Abstract: Artificial lenses and methods for optimizing vision in an eye of a patient comprising the steps of determining a target optical configuration including the optimum defocus and aberrations that the patients' eye should have in order to match or approximate the original optical configuration of the patient; determining the refractive change of the patient's eye required to achieve the optical configuration best corresponding to target optical configuration for the patient; and implementing the selected refractive change to achieve the target optical configuration.

Abstract: The present invention is an accommodative multifocal intraocular lens including an optical body, a haptic and a silicone connecting member, wherein the silicone connecting member is located between the optical body and the haptic, and combines the optical body and the haptic in an inserted manner through concave and convex grooves; two ends of the optical body are provided with concave grooves; an end, joined to the optical body, of the haptic is provided with a concave groove; two ends, along the width direction, of the silicone connecting member are provided with convex grooves, respectively, that is, a convex groove and a convex groove, respectively. The optical body in the present invention is a multi-focal optical zone, and the back-and-forth movement of the optical zone can effectively increase the change of the focal power of the multifocal lens.

Abstract: An accommodating intraocular lens (IOL) can be implanted either alone or as part of a two-part lens assembly. The IOL comprises an optic, a flexible membrane and a peripheral edge coupling the optic and the flexible membrane. The peripheral edge comprises an external circumferential surface having a height and a force transmitting area defined along a portion of the height of the external circumferential surface. A closed volume spaces apart the optic and the flexible membrane. The optic is axially displaced and the flexible membrane changes in curvature about a central axis when a radial compressive force is applied to the force transmitting area. A volume defined by the closed volume remains fixed when the optic is axially displaced and the flexible membrane changes in curvature and/or when the radial compressive force is applied to the force transmitting area.

Abstract: Delivery systems with telescoping capsules for delivering prosthetic heart valve devices and associated methods are disclosed herein. A delivery system configured in accordance with embodiments of the present technology can include, for example, a delivery capsule having a first housing, a second housing slidably disposed within a portion of the first housing, and a prosthetic device constrained within the first and second housings. The delivery capsule can further include first and second chamber defined in part by the first and second housings. During deployment, fluid is delivered to the first chamber to move the first housing distally over the second housing, thereby releasing a portion of the prosthetic device. Subsequently, fluid is delivered to the second chamber such that the first and second housings move together in the distal direction to release a second portion of the prosthetic device.

Abstract: A prosthetic valve comprises a first frame, defining an arrangement of cells; a second frame, a first protrusion, and a second protrusion. In an expanded state of the valve, the first frame is generally cylindrical and has an expanded width, and the valve defines a lumen having a first end and a second end. In a compressed state of the valve, the first and second frames are both generally cylindrical, and the first frame has a compressed width that is smaller than the expanded width. In the expanded state, the valve provides directional fluid flow through the lumen. The valve defines first and second coupling points, and an axis therebetween, the axis lying on a transverse cross-section of the first frame. The first and second coupling points couple the second frame to the first frame by protruding into respective first and second slots defined by the first frame.

Abstract: In one embodiment, a prosthetic valve can comprise a radially expandable and compressible frame, which can include a plurality of struts which are pivotally joined together without requiring individual rivets. In some embodiments, the struts are interwoven, and can be joined using integral hinges formed in the struts, such as by performing alternate cuts on the struts, bending the struts to form stopper tabs adjacent to joints and/or drilling holes in the struts to facilitate interconnecting struts at joints, or otherwise forming integral hinges and corresponding holes at junction points between the struts. In another embodiment, the frame comprises a plurality of inner struts and outer struts which are connected by a plurality of chains of interconnected rivets, avoiding the need to provide individual rivets at each junction between struts. In still another embodiment, separate hinges are provided to interconnect the struts.

Abstract: Apparatus is provided for use with a native valve of a heart of a subject. The apparatus includes: (1) an annular upstream support portion, comprising an expandable first frame, the upstream support portion configured to be placed against an upstream surface of the native valve; (2) a flexible polyester connector; and (3) an anchoring element, flexibly coupled to the upstream support portion by the connector, and configured to anchor the upstream support portion to the native valve by engaging tissue of the native valve.

Abstract: An implantable prosthetic valve includes an annular metallic frame and a valve assembly supported within the frame. The annular support frame is constructed with three longitudinal support beams of fixed length and web-like constructions that extend between and connect the support beams. The support beams are spaced apart in a substantially equidistant manner. The web-like constructions allow the annular support frame to be radially collapsible and expandable. Each support beam preferably has a column of pre-formed openings or bores extending along a length of the support beam. The valve assembly includes three valve leaflets, wherein each leaflet has opposing side portions and each side portion is paired with an adjacent side portion of an adjacent leaflet to form a commissure. The three commissures are secured to three respective support beams with stitching that extends through the leaflets and through the pre-formed openings or bores.

Abstract: Prosthetic heart valves and anchors for use with such valves are provided that allow for an improved implantation procedure. In various embodiments, an anchoring device is formed as a coiled or twisted anchor that includes one or more turns that twist or curve around a central axis. One or more arms attached to the frame of the valve guide the anchoring device into position at the native valve as it exits the delivery catheter, and the expandable prosthetic valve is held within the coil of the anchoring device. The anchoring device and the valve can be delivered together, simplifying the valve replacement procedure.

Abstract: The present disclosure describes tissue gripping devices, systems, and methods for gripping mitral valve tissue during treatment of a mitral valve and while a tissue fixation device is implanted in the mitral valve. The tissue gripping device includes a flexible member and one or more tissue gripping members coupled to one or more arms of the flexible member. The flexible member is formed from a shape-memory material, such as nitinol, and the tissue gripping member(s) are formed from a material that is more rigid than the shape-memory material. The tissue gripping member(s) are attached to the flexible member by threading or looping suture lines around and/or through the tissue gripping member(s) and the flexible member and/or by applying a cover material to the tissue gripping device to hold the tissue gripping member(s) against the flexible member.

Abstract: An implant system for restoring and improving physiological intracardiac flow in a human heart is provided including an implant for positioning at least partially in the atrium, partially within the atria-ventricular valve, and partially in the ventricle of the human heart and defining a contact surface; a base plate secured to the apex of the heart; a tether assembly connecting the implant to the base plate; and a sensor positioned on at least one of the implant, the base plate, and the tether assembly.

Abstract: A moldable sheet comprising malleable strands arranged in a substantially flat or planar configuration. The moldable sheet can be manipulated into a variety of shapes and is capable of maintaining the manipulated shape. Broken and fractured bones and bone fragments can be held together by wrapping a moldable sheet around the exterior of the break or fracture area. The moldable sheet can secure the ends of the bone for healing and can be incorporated into the new bone growth. The structure of the moldable sheet can be such that electromagnetic waves, such as those used with medical or security scanning equipment, are able to pass through pores in the device. This can make the moldable sheet radiolucent.

Abstract: Disclosed herein are an implant with an attachment feature and a method for attaching to the same. The implant may include a cavity with a porous layer disposed within a non-porous layer wherein the non-porous layer defines a chamber. The chamber may receive and confine liquefiable material and direct liquefiable material to permeate through the porous layer. A method of attaching a device to the implant may include liquefying a liquefiable portion of the device and allowing the liquefied material to interdigitate with the second layer and then solidify to prevent pullout.

Abstract: A bone implant including a wire mesh support frame (120A) having a plurality of interconnected wire members and at least two fastening points in the form of retention eyelets (140A) connected to the support frame by deformable retention arms (138A), and a biocompatible plate (112) formed about the support frame, the plate having at least two open cavities (116) therein, wherein each of the retention arms extends out of the plate from or into one of the open cavities. A method for correcting a bone defect in a patient, a mesh support frame for use in a bone implant, and a method of fabricating a bone implant are also provided.

Abstract: An augment for supporting an acetabular shell at an acetabulum of a hip bone. In some examples, the augment can include a body having a first surface and a second surface opposite the first surface. The body can extend from a first end portion that is adapted to be fixed to an acetabular shell, to a second end portion. The body can include a first hole and a second hole, each of the first and second holes extending through the body from the first surface to the second surface. The body can be formed of a porous material that promotes boney ingrowth and can further include a trim marker located in between the first hole and the second hole.

Abstract: A method of anatomically positioning screw holes in an acetabular implant that can be used in surgery, such as a total hip arthroplasty. In some examples the method can be used to position holes in a shell of the implant. The method can include, for example, obtaining anatomic data including data defining an arch of bone behind an acetabulum of the living being, the arch of bone extending from a superior anterior portion to an inferior posterior portion of the acetabulum. The method can further include positioning a first series of holes along a first arched line within the acetabular shell, the first arched line determined based on the anatomic data for the arch of bone proximate the acetabulum of the living being.

Abstract: The present invention relates to a partial joint replacement (1000), encompassing a shell-like segment (100) with a concave inner contour (3) for the arrangement on at the bone structure of a patient, wherein the segment (100) comprises a lateral section (5) and a medial section (7) along a longitudinal direction (x), and wherein the outer contour (1) of the segment (100) comprise in longitudinal direction (x) at least one inflection point (9).

Abstract: There is provided a tibial component comprising: a tibial tray with an inferior side; and a support member connected to the inferior side of the tibial tray, the support member having a stem portion, the support member further comprising at least one opening. In one embodiment, the at least one opening is constructed and arranged to receive a sawblade or an osteotome. In another embodiment, the at least one opening is comprised of solid material but is radio-lucent. In yet another embodiment, the at least one opening is comprised of solid material and is frangible.

Abstract: There is provided a tibial component comprising: a tibial tray with an inferior side; and a support member connected to the inferior side of the tibial tray, the support member having a stem portion, the support member further comprising at least one opening. In one embodiment, the at least one opening is constructed and arranged to receive a sawblade or an osteotome. In another embodiment, the at least one opening is comprised of solid material but is radio-lucent. In yet another embodiment, the at least one opening is comprised of solid material and is frangible.

Abstract: A bicondylar knee implants with improved fixation means for resurfacing only the weight-bearing surface of the femoral medial and lateral condyles, while preserving the cruciate ligaments and avoids displacing the patella. The inventive device includes metallic convex articular surfaces for resurfacing the medial and lateral femoral condyles, and concave multifacial non-articular surfaces to be affixed to the resected distal surfaces of the femur. The prosthesis provides claws situated at the anterior and posterior ends of the medial and lateral metallic condyles, which will firmly attach the implant against the resected femoral condyle. The prosthesis is designed to be implanted through a direct lateral approach and does not resurface the femoropatellar joint. Furthermore, a minirobot or electromechanical actuator is used to perform the femoral and tibial bone cuts using electromagnetic bone chipper.

Abstract: Disclosed is a medical device having a first implant portion having a proximal end, a second implant portion connected to the first implant portion, the second implant portion having a distal end, and a driver assembly removably connected to the distal end, the driver assembly comprising a drill connected to the distal end at a connection.

Abstract: Intervertebral endoprosthesis discs suitable for surgical implantation between two vertebrae having and methods thereof. The prosthetic disc may have an endoprosthesis body including an anterior region and a posterior region designed to be positioned between a first vertebra and a second vertebra with a first and second movable insert positioned rotatably in anterior cavities and is rotatable to adjust the fasteners.

Abstract: A spinal implant formed from a hinged distractor having an upper and lower support body that is hinged by use of pinions. An insert body is constructed and arranged to slide between the section to expand the height and to maintain a space therebetween. The insert body may include a leading edge that is tapered to allow ease of insertion. A trailing edge of the insert body includes a pin to allow ease of insertion along a curvature path.

Abstract: The present invention provides an expandable fusion device capable of being inserted between adjacent vertebrae to facilitate the fusion process. The expandable fusion device may include first and second endplates, a translation member configured to expand an anterior side and/or posterior side of the device, a plurality of joists configured to connect the first and second endplates to the translation member, and first and second actuation members disposed internally to the device such that openings on a back side of the device can be used to expand or compress the anterior side, the posterior side, or both and such openings may also be used to introduce graft material into the device.

Abstract: A cervical plate formed from an expandable clip that is drawn toward a plate by use of a draw screw coupled to a draw bar. The draw bar is placed in an aperture having engagement with an angular surface that operates in conjunction with a proximal and distal end of the clip, which engages a tab to cause expansion when the draw screw engages the draw bar across a plate.

Abstract: Interbody spacers are expandable horizontally and vertically by an application of axial force, and lockable in an expanded configuration. The spacers include support members interconnected to end bodies by pivotable link members. The spacers are introduced between vertebral bodies in a compressed configuration and expanded to fill the intervertebral space and provide support and selective lordotic correction. Graft material may be introduced into the expanded spacer. Provisional and/or supplementary locking means lock the spacers in the expanded configuration. Embodiments of the spacers include symmetrically and asymmetrically configured spacers. Methods of expansion include symmetric expansion or asymmetric expansion along each of two directions.

Abstract: An intervertebral implant includes a three-dimensional body and a securing plate. The three-dimensional body includes a front surface and a rear surface. The three-dimensional body further includes a plurality of boreholes for accommodating fixation elements. The intervertebral implant also includes a front plate disposed at the front surface of the three-dimensional body and has a plurality of boreholes. A securing plate can be fastened to the front plate.

Abstract: An intervertebral device comprises a plurality of struts that are rotatably associated with each adjacent strut to form a modifiable inner volume V for bone graft containment.

Abstract: An implantable device includes a barrel. The barrel has a first portion and a second portion. The implantable device includes a first plate having multiple projections extending from one side of the first plate, where the first plate is configured to movably couple to the first portion of the barrel. The implantable device includes a second plate having multiple projections extending from one side of the second plate, where the second plate is configured to movably couple to the second portion of the barrel. The barrel is configured to transition from a collapsed form having a first height to an expanded form having a second height, where the second height is greater than the first height.

Abstract: To reduce the stress of a patient as much as possible during a percutaneous spine surgery for inserting an interbody cage between two vertebrae, between which the intervertebral disk was damaged and was therefore removed, a guide sleeve is provided for the spine surgery, which is characterized by a non-cylindrical jacket. A kit is further provided for spine surgery with at least one guide sleeve of the above-mentioned type and a dilator, having an outer contour that is adapted to the contour of the lumen of the guide sleeve. A kit for spine surgery is further provided including a guide sleeve and an interbody cage, which is to be inserted through this guide sleeve. The lumen of the guide sleeve is adapted to a maximum cross-sectional contour of the interbody cage.

Abstract: A system for performing spinal surgery includes an assembly of one or more manipulation instruments for manipulating and positionally adjusting one or more implants within a spinal disc space. The assembly has a one or more of grasping and manipulating features with actuators and includes a shim instrument that has a body with at a wedge shaped spacer shim at its distal end and in an inverted orientation.