Abstract: Embodiments described herein are related to pellets that are placed within an extraction site that is in need of bone augmentation and preservation. The pellets are typically cylindrical in shape and comprise a material and a polymer coating. The goal of the pellets are to encourage sufficient new bone growth that jaw bone deterioration is prevented. The pellets create, arrange, and assemble an ideal growth environment for new bone growth to rapidly grow and preserve the original contours of an individual's jaw bone.

Abstract: A socket grafting plugs system for use in a socket grafting process. Each socket grafting plug has a first cross section, a second cross section parallel to the first cross section and a body portion extending between the first cross section and the second cross section. The first cross section belongs to a group of first plug sections with at least a combination of three different shapes with three different sizes.

Abstract: Methods for manufacturing anatomical healing caps, including forming an anatomical healing cuff body for a given tooth position, the anatomical healing cuff body having a cross-section and an exterior surface so that the anatomical healing cuff body provides substantially custom filling of at least an emergence portion of a void where a natural tooth once emerged from the void or where a tooth would have emerged from a void of the given tooth position, and forming both lateral buccal and lingual handle extensions extending from the anatomical healing cuff body so that the manufactured anatomical healing cap includes a laterally extending buccal handle extension and an oppositely disposed laterally extending lingual handle extension, the buccal and lingual handle extensions being integrally formed with the healing cuff body. The healing caps can be formed using a casting jig, by machining, by 3D printing, or other suitable methods.

Abstract: A set of instruments with portions shaped and sized to engage specific portions of a dental implant is provided. Each of the instruments includes a tip on an end of a shank, the tip including an arcuate portion transverse to a longitudinal axis of the end of the shank. The arcuate tip portion may be crescent or hook shaped.

Abstract: A method of using AR for dentistry and orthodontics is provided. An image of a dental arch is received, the image having been generated by an image capture device associated with an augmented reality (AR) display. A processing device registers the image to previous image data associated with the dental arch, compares one or more areas of the dental arch from the image to one or more corresponding areas of the dental arch from the previous image data, determines a position of an area of interest on the dental arch based on the comparing, generates a visual overlay comprising an indication of the area of interest, and outputs the visual overlay to the AR display, wherein the visual overlay is superimposed over a view of the dental arch on the AR display at the position of the area of interest.

Abstract: The present invention provides a dental mill blank having reduced cracks and that excels in mechanical strength and aesthetic quality. The present invention relates to a dental mill blank comprising an inorganic filler and a polymer, and having a porosity of 25 to 35 volume % after 2-hour ashing at 600° C. In the dental mill blank, the inorganic filler preferably comprises an inorganic filler (A) and an inorganic filler (B), and the dental mill blank preferably satisfies the following formulae (I) and (II), 0.12?a?0.70??(I) 3?b/a??(II), where a is an average primary particle diameter of the inorganic filler (A) in micrometers, and b is an average primary particle diameter of the inorganic filler (B) in micrometers. Preferably, the inorganic filler (A) and the inorganic filler (B) have a volume-to-volume content ratio (A)/(B) of 5/95 to 50/50.

Abstract: Embodiments of a floss strip and methods of using the same are disclosed herein. The floss strip can include a flossing filament. The flossing filament can have a first end and a second end. The flossing strip can include a first anchor coupled to the flossing filament at the first end of the flossing filament. The flossing strip can include a second anchor coupled to the flossing filament at the second end of the flossing filament. The flossing filament can couple the first and second anchors. The flossing strip can include a tensioning member attached to the flossing filament at an intermediate location between the first anchor and the second anchor.

Abstract: A cleaning device (10) comprising: a body portion (12); a nozzle member (14) mounted on the body portion and comprising a nozzle head (16), wherein the nozzle member is configured to allow passage of liquid and/or air from a reservoir in the body to the nozzle head; and an orifice (40) in the nozzle head configured to allow the liquid and/or air to exit the nozzle head, wherein the orifice is configured to shape the exiting liquid and/or air into at least one liquid sheet having a length greater than a width at a target cleaning distance.

Abstract: An oral cavity washing device includes a housing, a tubular storage space formed in the housing to store a liquid, and a pump housed in the housing to discharge the liquid. The housing includes a peripheral wall section constituting at least part of a peripheral wall of the storage space and having a supply port for supplying the liquid into the storage space, and a lid disposed at one end of the storage space to be able to entirely open and close a largest opening that is larger in area than any other opening in the housing.

Abstract: The present invention describes a method for a U-shaped teeth brush device having a conformable shape adjusting U-shaped teethbrush module and one or more individual tooth brushes coupled to the power drive mechanism, each brush having a sensor, piezoelectric crystal and transducer and each tooth brush having a block anchor coupled to the power drive, under smart controls, an electronic control system for sensing individual tooth pressure and controlling motor transmission of vibration to prior positioned brushes, whereby a users unique mouth features can be accounted for by adjusting U-shape distal ends to fit through the users mouth and align with users teeth arch for programmatically brushing more than one tooth simultaneously.

Abstract: The present disclosure relates to the technical field of electric toothbrushes, and in particular to an electric toothbrush motor. The electric toothbrush motor comprises a mounting shell, an end cover, conductors, a rotor assembly and a stator assembly, wherein the rotor assembly and the stator assembly are fixedly arranged in an accommodating cavity of the mounting shell through the end cover. The first magnetic steel sheets are added to the rotor assembly, the second magnetic steel sheets are added to the stator assembly, each first magnetic steel sheet is placed at the middle part of an interval between the two second magnetic steel sheets, and by the above manner, the relative positions of the rotor assembly and the stator assembly are fixed, so that the response speed is increased, the vibration frequency is high, and the service life is prolonged.

Abstract: The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to medical devices, systems, and methods for tightening, fastening, or anchoring in tissue. In one example, a system for tightening, fastening, or anchoring in tissue, may comprise a spring coil having a distal end, a stressed configuration, and an unstressed configuration; and a restraining tube having a lumen extending along a length of the tube. The spring coil may be removably receivable within the lumen to restrain the spring coil in the stressed configuration. Other embodiments are contemplated.

Abstract: A tubular tissue graft device is provided comprising a tubular member and a restrictive fiber matrix of a bioerodible polymer about a circumference of the tubular tissue. The matrix may be electrospun onto the tubular tissue. In one embodiment, the tubular tissue is from a vein, such as a saphenous vein, useful as an arterial graft, for example and without limitation, in a coronary artery bypass procedure. Also provided is method of preparing a tubular graft comprising depositing a fiber matrix of a bioerodible polymer about a perimeter of a tubular tissue to produce a tubular tissue graft device. A cardiac bypass method comprising bypassing a coronary artery with a tubular tissue graft device comprising a vein and a restrictive fiber matrix of a bioerodible polymer about a circumference of the vein also is provided.

Abstract: Described herein are devices, systems, and methods for modifying blood flow and improving tissue oxygenation in an individual. More specifically, described herein are flow modifying implants, delivery systems, and methods of treatment using flow modifying implants. Also described herein are methods for preventing reperfusion injury in an individual using a flow modifying implant to prevent the reperfusion injury.

Abstract: The present disclosure relates generally to methods and apparatus for endovascular replacement of the aortic valve, aortic root, and ascending aorta. The present subject matter includes various embodiments of methods and apparatus for connecting the coronary arteries to an endovascular assembly including an aortic valve device (AVD), an aortic root graft, and an ascending aortic stent graft. The present subject matter provides for replacement of the aortic valve, aortic root, and ascending aorta without requiring open-heart surgery. It provides different options for connections to the coronary arteries and for assembling the aortic valve device and the aortic root graft.

Abstract: Various aspects of the present disclosure are directed toward implantable medical devices that include a frame and a tubular member attached to the frame. The tubular member includes one or more fibrils or a strength in alignment with one or more struts of the frame.

Abstract: The disclosure describes implantable bioprosthesis and constructs having an implantable woven ribbon with at least one integrated suture.

Abstract: An example medical device is disclosed. The medical device includes an implant delivery system having a delivery shaft including a proximal portion and a distal portion and a detachable frame coupled to the distal portion of the delivery shaft. The detachable frame includes a body portion and a plurality of attachment arms extending away from the body portion. The plurality of attachment arms are configured to be attached to an implant and the detachable frame is configured to detach from the delivery shaft in vivo.

Abstract: The invention relates to a prosthesis for supporting a breast implant comprising: a reinforcement part configured to receive a curved lower portion of a breast implant, the reinforcement part having an elongation under 50N in the vertical direction of E1, a fixation part intended to be fixed to the pectoral muscle, the fixation part having an elongation under 50N in the vertical direction of E2, and a transition part connecting together the reinforcement part and the fixation part, said transition part having an elongation under 50N in the vertical direction of E3, wherein E3 is greater than E1 and greater than E2.

Abstract: A deformable intraocular lens (IOL) comprises a deformable optic, having an annular edge around its periphery, and at least two haptics, each having a proximal portion and a distal portion relative to the optic. Each haptic extends from a different position on the annular edge of the optic and can be compressed. The IOL further comprises at least one tab extending from the annular edge of the optic at a position different from the proximal portion of each of the haptics. The or each tab can adjust the folding characteristics of the IOL, which in turn can control the speed and orientation of the IOL on injection into a patient's eye and ensure greater reliability of desired injection.

Abstract: An accommodating intraocular lens assembly can include first stanchions, a forward optic, second stanchions, an intermediate member, third stanchions, fourth stanchions, and an aft optic. Each stanchion can extend between a base end and a distal end. The forward optic can be connected with the distal ends of the first stanchions. The intermediate member can be connected with the distal ends of the second stanchions and of the third stanchions. The aft optic can be connected with the distal ends of the fourth stanchions.

Abstract: An apparatus (200, 200A, 200B, 200C) has central lens body (212, 212A, 212B, 212C) for providing vision correction for a patient. The lens body (212, 212A, 212B, 212C) has an initial index of refraction and is formed from at least one material configured to have a second index of refraction when subjected to a laser and/or radiation.

Abstract: A valve catheter is advanced through a patient's vasculature while a prosthetic heart valve is attached to flexible extensions along a distal end thereof. The valve catheter is advanced through a tubular sleeve for exposing the prosthetic heart valve and allowing the prosthetic heart valve to self-expand while the extensions remain attached to the prosthetic heart valve. A release mechanism on a handle portion is actuated for releasing the prosthetic heart valve from the extensions, thereby implanting the prosthetic heart in a native heart valve. If the operator is not satisfied with the initial expansion, the prosthetic heart valve may be reoriented before release from the extensions by retracting the prosthetic heart valve back into the tubular sleeve, adjusting the orientation of the prosthetic heart valve and then re-advancing the valve catheter from the tubular sleeve for allowing the prosthetic heart valve to re-self-expand at a more desirable location.

Abstract: Described embodiments are directed toward prosthetic valve leaflets of a particular shape that allows redundant coaptation height in the leaflets when a planar segment is present in each leaflet.

Abstract: The invention relates to a transcatheter heart valve replacement (A61F2/2412), and in particular a side delivered transcatheter prosthetic heart valve having a collapsible inner flow control component, and an outer annular support frame having compressible wire cells that facilitate folding flat along the z-axis and compressing the valve vertically along the y-axis, or orthogonally to the central axis of the flow control component, allowing a very large diameter valve to be delivered and deployed to the tricuspid valve from the inferior vena cava or superior vena cava, or trans-atrially to the mitral valve, the valve having a height of about 5-60 mm and a diameter of about 25-80 mm, without requiring an oversized diameter catheter and without requiring delivery and deployment from a catheter at an acute angle of approach.

Abstract: A prosthetic mitral valve includes an anchor assembly, a strut frame, and a plurality of replacement leaflets secured to the annular strut frame. The anchor assembly includes a ventricular anchor, an atrial anchor, and a central portion therebetween. The ventricular anchor and the atrial anchor are configured to flare radially outwards relative to the central portion. The annular strut frame is disposed radially within the anchor assembly and is attached to the anchor assembly. The central portion is configured to align with a native valve orifice and the ventricular anchor and the atrial anchor are configured to compress native cardiac tissue therebetween.

Abstract: The present disclosure pertains to introducer sheaths with an inner liner for percutaneous insertion of a medical device into a patient. The introducer sheaths can further have a tubular layer and an outer layer. The tubular layer can be a metal sleeve having a plurality of slots. The present disclosure also discloses embodiments of catheter-based prosthetic heart valves, including, prosthetic heart valves having sealing members configured to seal the interface between the prosthetic valve and the surrounding tissue of the native annulus in which the prosthetic valve is implanted.

Abstract: Embodiments of a crimping device for crimping a radially expandable and compressible prosthetic valve are disclosed. A crimping device can comprise a housing configured to receive a prosthetic valve in a radially expanded state. The housing member can include a funnel segment and an outlet in communication with the funnel segment. The crimping device can further comprise an actuator rotatably coupled to the housing, wherein rotation of the actuator relative to the housing causes the prosthetic valve to move axially through the funnel segment such that at least a portion of the prosthetic valve compresses radially by engagement with the funnel segment and exits the crimping device via the outlet.

Abstract: A bendable medical instrument including: a handle at a proximal end of the bendable medical instrument, a modular distal shaft including a plurality of vertebrae configured to bend and situated near a distal end of the bendable medical instrument, a bendable internal rod disposed through at least some of the plurality of vertebrae, the bendable internal rod having a modular cell structure, and a distal tip coupled to the modular distal shaft at the distal end. The plurality of vertebrae configured to bend to position the distal tip in a patient and the bendable internal rod configured to bend with the plurality of vertebrae.

Abstract: This document provides devices and methods for the treatment of heart conditions such as valvular stenosis. For example, this document provides devices and methods by which a guide catheter can align itself with a blood flow stream to thereby help direct a guidewire or other elongate device transmitted from the guide catheter through an orifice of a heart valve.

Abstract: An implantable prosthetic device has a coaption element and at least one anchor. The coaption element is configured to be positioned within the native heart valve orifice to help fill a space where the native valve is regurgitant and form a more effective seal. The coaption element can have a structure that is impervious to blood. The coaption element can be connected to leaflets of the native valve by the anchor.

Abstract: Methods and devices for the treatment of cardiac valve dysfunction through the placement of lines and anchors. The lines and anchors can form artificial chordae between valve leaflets and the ventricular wall or papillary muscles or connect the two valve leaflets together. The methods and devices offer a mechanism for performing this technique with the heart still beating, and allows for the placement of multiple lines with a single device.

Abstract: A method for manufacturing a personalized naturally designed mitral valve prosthesis to precisely fit a specific patient for which the valve prosthesis is made for is provided. The method includes measuring size and shape of a mitral valve of the specific patient by using imaging methods, calculating geometry and dimensions of annular ring, leaflets and chords per the specific patient based on validated algorithms, and cutting and connecting the annular ring, leaflets and chords to form a personalized prosthesis mitral valve.

Abstract: A testing apparatus is disclosed herein for testing properties of a prosthetic device. The testing apparatus may comprise a dual-drive pulsatile flow tester with the ability to determine coaptation of valve leaflets of a prosthetic device. The testing apparatus may be able to test prosthetic heart valves and reproduce physiological conditions of a prosthetic heart valve.

Abstract: The devices and methods described herein may be used to restore left ventricular function to address mitral valve regurgitation. One variation of an implant comprises a plurality of tethered anchors and a plurality of force-distribution members slidably disposed on the tether between the anchors. One or more of the force-distribution members can comprise a bioabsorbable material. Methods comprise deploying the implant to cardiac tissue, cinching the implant to its hard stop (e.g., where further cinching does not cause further tissue tightening), providing a pre-selected amount of slack to the implant after it has been cinched to its hard stop configuration, and securing a lock member on the tether. Also disclosed herein are lock member deployment catheters that provide a pre-selected amount of tether slack as it secures a lock member on the tether.

Abstract: In one embodiment, the present disclosure relates to an acetabular implant system with a liner and a sleeve. The liner includes a convex outer surface shaped to correspond to an interior of an acetabular cup and has an equatorial region and a polar region. The convex outer surface includes a plurality of liner engagement features thereon. The sleeve includes an inner surface with a plurality of sleeve engagement features thereon. The inner surface of the sleeve is sized to be flush with the convex outer surface of the liner. When the sleeve is engaged with the liner, the liner engagement features engage the sleeve engagement features.

Abstract: According to one example, a tibial prosthesis that can include a tibial bearing component, tibial baseplate, an insert and a fastener. The tibial bearing component can have medial and lateral proximal articular surfaces and an opposing distal surface. The tibial bearing component can define at least one recess therein with the recess having an opening at a periphery of the tibial bearing component. The tibial baseplate can be coupled to the tibial bearing component on the proximal surface thereof and having a distal surface configured to be disposed on a resected proximal surface of a tibia. The insert can be configured to be disposed within the recess and can engage the tibial baseplate and the tibial bearing component. The fastener can be insertable into the tibial bearing component and can be configured to retain the insert to the tibial baseplate.

Abstract: An implant is disclosed that has a base member, an articulating member, and a coupling portion that secures the base member to the articulating member. The implant can be a shoulder implant (100, 200, 300) that has a baseplate (102, 230, 310), an articulating component (104, 210), and a fixation component (106, 270, 342). The baseplate includes a first side (110, 234, 314) with a projection (108, 240, 320) that has a first Morse taper and may be offset from a center line of the baseplate and a second side (116, 236, 316) that has a post or stem (114, 250, 330) that is offset from the center line of the baseplate. The articulating component includes a cavity (122, 220) with a second Morse taper that is offset from a center line of the articulating component. The articulating component is attachable to the baseplate when the projection is received in the cavity of the articulation component.

Abstract: The present invention relates to a three-dimensional multiphasic synthetic tissue scaffold comprising first, second and third compartments, wherein: each said compartment comprises distinct microstructural, and/or chemical, and/or mechanical properties, and is connected with at least one other compartment of the scaffold via a continuous interface; the tissue scaffold is porous; and the external morphology of the tissue scaffold mimics that of a mammalian joint or a component thereof. The invention further relates to a method for producing the three dimensional multiphasic synthetic tissue scaffold using a polymeric material, the method comprising using a three-dimensional (3D) bioprinter to print the tissue scaffold by continuously deposit the polymeric material onto a platform until the tissue scaffold is produced in its entirety.

Abstract: A laterally deflectable asymmetric implant for implanting into a body may comprise a deflectable piece having distal and proximal ends and assuming a straightened insertion state. The backbone may abut or interconnect with said deflectable piece at the distal end of the deflectable piece. In a fully deflected state the implant may define an asymmetric shape, e.g. a D-shaped loop, defining an at least partially enclosed volume. The deflectable piece may comprise a sequence of segments interconnected at effective hinges. Longitudinal pressure applied to the proximal end of the deflectable piece (or applied to the backbone in an opposite direction) may cause relative longitudinal movement between the backbone and the proximal end of the deflectable piece and may generate outward horizontal movement of the deflectable piece away from the backbone. In one embodiment, the implant is implanted using lateral access into an anterior zone of a vertebra and deployed posteriorly.

Abstract: An expandable vertebral body device, system, instrument, and methods of assembly and using the device, system, and instrument are disclosed. The vertebral body device includes a body with a first end and a second end, a first rotating member rotatably coupled to the first end, a second rotating member rotatably coupled to the second end, a first extension member moveably coupled to the first end, and a second extension member moveably coupled to the second end. The expandable cage system comprises a vertebral body device and an insertion instrument. Methods for assembling and using the vertebral body device and instrument are also disclosed.

Abstract: A corpectomy cage includes a main body, a first end cap, and a second end cap. The main body is shaped as a hollow rectangular prism, and includes a first end and a second end. The first end has a plurality of first receivers formed therein, and the second end has a plurality of second receivers formed therein. The first end cap includes a plurality of first legs configured to be received within respective first receivers to removably engage the first end cap with the first end of the main body. Similarly, the second end cap includes a plurality of second legs configured to be received within respective second receivers to removably engage the second end cap with the second end of the main body. Each of the end caps further includes a plurality of teeth arranged opposite the plurality of legs.

Abstract: An intervertebral implant device includes a first plate having a first fixation component; and a first set of outwardly extending projecting members. The device also includes a second plate having a second fixation component; and a second set of outwardly extending projecting members that compliment an alignment with the first set of outwardly extending projecting members. The device also includes a core member that extends through the first plate and the second plate. The core member limits movement of the first plate away from the second plate; and a connecting member that connects to the core member.

Abstract: An expandable fusion device may include a first endplate and a second endplate. The expandable fusion device may also include first and second ramps configured to mate with both the first and second endplates. An inserter instrument includes an outer shaft having a bore extending longitudinally therethrough and an inner shaft extending through the bore in the outer shaft. The outer shaft is configured to engage the first or second opening in the second ramp, and the inner shaft is configured to engage the corresponding first or second opening in the first ramp to control implant height and/or lordotic angle.

Abstract: A spinal implant is provided and includes a body portion defining a longitudinal axis. The body portion includes a distal end portion, a proximal end portion, opposed side surfaces that extend between the distal and proximal end portions, and top and bottom surfaces configured and adapted to engage vertebral bodies. The top and bottom surfaces have a surface roughness between 3-4 ?m. A cavity extends through the top and bottom surfaces defining a surface area that is at least 25% of a surface area of the top surface or the bottom surface. First orifices are defined through the top surface and second orifices are defined through the bottom surface. The second orifices are connected to the first orifices by a plurality of channel.

Abstract: A tool for delivery and/or compaction of bone graft material includes a cannula with an inner lumen extending along a longitudinal axis from a hopper end of the cannula to a delivery tip of the cannula. A hopper with an internal volume for storing bone graft material is connected to the hopper end of the cannula with the internal volume of the hopper in communication with the inner lumen of the cannula for delivery of bone graft material from the hopper to the delivery tip of the cannula. An output shaft within the inner lumen extends along the longitudinal axis. The output shaft includes a helical screw thread extending radially outward from the output shaft toward an inner surface of the cannula. An actuator is connected to the hopper and to the output shaft to drive the output shaft rotationally relative to the hopper and to the cannula.

Abstract: A dilation introducer for orthopedic surgery is provided for minimally invasive access for insertion of an intervertebral implant. The dilation introducer may be used to provide an access position through Kambin's triangle from a posterolateral approach. A first dilator tube with a first longitudinal axis is provided. A second dilator tube may be introduced over the first, advanced along a second longitudinal axis parallel to but offset from the first. A third dilator tube may be introduced over the second, advanced along a third longitudinal axis parallel to but offset from both the first and the second. An access cannula may be introduced over the third dilator tube. With the first, second, and third dilator tubes removed, surgical instruments may pass through the access cannula to operate on an intervertebral disc and/or insert an intervertebral implant.

Abstract: A surgical instrument includes a housing, an outer shaft, an inner shaft, a trial sizer, a rod, and a head. The outer shaft is operatively coupled with the housing such that rotation of the housing causes axial displacement of the outer shaft. The outer shaft includes a keel cutter configured to form a channel in a vertebral body. The inner shaft disposed within the outer shaft. The trial sizer is configured to be received in intervertebral space. The trial sizer includes a pair of wings transitionable between a retracted position and an extended position in which the pair of wings extends transversely outward. The head is connected to the rod, wherein the head is operatively coupled with the pair of wings such that axial displacement of the rod causes transition of the pair of wings between the retracted and extended positions.

Abstract: A prosthetic joint system for users comprising a housing having an interior cavity, a center axis in said interior cavity, and an attachment means for fixedly connecting said housing to said user; an inner cylinder disposed in said housing interior cavity wherein said inner cylinder rotates around said center axis of said housing; an appendage attached to said inner cylinder; a sensor system attached to said appendage; and a dampening system, having a power source, in communication with said sensor system, said inner cylinder, and said housing for controlling dampening of the rotation of said inner cylinder around said center axis of said housing.

Abstract: Described here are prosthetic systems, devices, and methods of use therefor. Generally, a prosthesis may be configured to set a resistance to rotation of a prosthetic joint based on a phase of gait. The prosthesis may include a first cylinder, a first piston slidable within the first cylinder, a fluid sump, and a fluid circuit. The fluid circuit may include a plurality of interconnected fluid channels having a unidirectional variable-resistance valve and a set of check valves that are configured to provide unidirectional flow through the valve during piston compression and extension.