Abstract: A medical marking device, consisting of a radiotransparent plate having a plurality of radiopaque elements embedded therein in a predefined pattern. The device also has a sigmoid mounting arm having a first end connected to the radiotransparent plate and a second end containing one or more fastening receptacles.

Abstract: A method is used to calibrate a light unit, including at least one light source, the light unit being part of a medical imaging apparatus. In an embodiment, the method includes positioning a calibration phantom at a calibration position, in particular a first calibration position; arranging the light source so that its beam illuminates the photodetector at least partially; starting or continuing the recording of light intensities using the photodetector; modulating the signal of the light source at least once; rotating the light beam around a given rotation axis while recording the rotational position; synchronizing the time values of the rotational position of the light beam and the acquired signal intensities using the modulation of the light signal; and mapping the rotational position, in particular the rotation angle, of the light beam to a spatial position using the light intensities recorded by the photodetector.

Abstract: A surgical instrument with a handle and a blade disposed thereon having a concavely developed cutting edge, wherein the blade comprises a plane, wherein the surgical instrument comprises ultrasound visibility-enhancing media.

Abstract: An operating room display system includes a display device, a sensor coupled to the display device and configured to detect a presence of a medical device disposed within the operating room, a communications interface communicatively coupled to the display device and the sensor, and a memory communicably coupled to the communications interface, wherein the memory comprises a device information module. The display device is configured to show a display providing information from the device information module to a user in the operating room regarding the medical device detected by the sensor.

Abstract: Two new burs to be used in dentistry applications. The two burs are used one after the other to create a natural anatomy in restorations of teeth. One of the burs also reduces the need for anesthetic by providing for minimal contact with the dentin while removing the enamel when cutting into a tooth.

Abstract: Strategies that reduce shrinkage and ultimately warping of parts that are directly fabricated from photopolymer resins. This increases the accuracy of directly fabricated parts, which is essential for patient specific applications. Implementing these strategies can reduce the need for directly fabricated parts to have supporting structures, which can reduce pre-processing and post-processing steps and facilitate an easier route for production level scale of additive manufacturing.

Abstract: Customized dental implants feature enhanced osseointegrable qualities by manufacturing the implant post with osseointegrable material and preparing a larger post body, including a portion to cover a prepared bone surface, to integrate with a jawbone. Resultant implants are more durable and provide a better fir into the oral cavity. Various implant shapes and designs are disclosed.

Abstract: An oral irrigator includes a sprayer, a spray lance, a control switch, a vessel, a water pipe and a water volume stepless adjustment device. The water volume stepless adjustment device includes an adjusting switch, a controller and a signal output device. A signal output by the controller can be continuously adjusted for adjusting the adjusting switch to continuously adjust the magnitude of pressure of a fluid sprayed from the spray lance. When a user uses the oral irrigator, the user can adjust the water pressure according to personal tolerance and preferences until feeling most comfortable, thereby greatly enhancing the cleaning effect and comfort of the oral irrigator in a using process. The oral irrigator can also be connected to an oral observation instrument, so that under direct vision, the water volume is adjusted, the teeth and the oral cavity are cleaned, and the cleaning process can be shot and photographed.

Abstract: Described herein are systems and methods for providing personalized oral irrigation. One variation of a system for personalized oral irrigation comprises a fluid reservoir and a customized oral insert in fluid communication with the fluid reservoir. The oral insert comprises an arrangement of fluid openings positioned based on the individual oral or dental structures of a user's teeth to provide a customized fluid flow over the user's teeth. Also described herein are methods for generating an arrangement of fluid openings in a customized oral insert.

Abstract: A measuring system for analysis of space for dental implant restoration comprises a first measuring assembly for measuring a mouth opening degree and a first gap of plural missing teeth, a second measuring assembly for measuring a second gap of a single missing tooth and an occlusal distance, and a third measuring assembly for measuring a transgingival depth, wherein each of the first measuring assembly, the second measuring assembly and the third measuring assembly comprises a connecting rod and a measuring head disposed at an upper end of the connecting rod. A measuring method for analysis of space for dental implant restoration using the aforesaid measuring system for analyzing is further disclosed.

Abstract: Methods and systems for assessing the treatment effectiveness of oral care products. An apparatus for assessing the effectiveness of the sensitivity improving, stain prevention, and/or stain removal capability of an oral care product. Apparatuses for identically applying an oral care product to two or more surfaces simulating an oral cavity surface, such as a tooth surface.

Abstract: The invention relates to an occlusive cuff (1) for selectively occluding an anatomical duct (2), comprising: a band (10) suited to surrounding said anatomical duct (2), provided with a closing device suited to maintaining the band wound upon itself over a determined length (L10), and an inflatable reservoir (11) arranged on an inner face of the band (10), said cuff being characterised in that the inflatable reservoir (11) extends over only a part (L11) of the length (L10) of the band (10), another part (L13) of said length (L10) defining a free inner surface (13) of the band configured to form a bearing zone for the anatomical duct, such that when the band (10) is maintained wound upon itself by the closing device, the inflatable reservoir (11) is opposite said free inner surface (13) of the band.

Abstract: This three-dimensional knitted textile insert is obtained in a single step by warp knitting technology, on a double-needle Raschel machine or on a crocheting machine. It includes in the production direction at least two tubes extending parallel to one another, and separated from one another by a binding area at the level of which the sheets resulting from the knitting are interlinked.

Abstract: A peripheral vascular filter according to some aspects of the invention includes a filter body forming a cavity therein, the filter body having a proximal end and a distal end in a length-wise direction of the peripheral vascular filter, the filter body having an opening in the proximal end thereof; a spring system arranged proximal to the filter body and in mechanical connection with the filter body and with a filter wire, the spring system being stretchable along the length-wise direction; a plurality of retractor wires, each retractor wire having a distal end connected to the filter body, and a proximal end connected to spring system. In a deployed configuration, the spring system absorbs forces applied to the filter wire proximal to the filter body to prevent the peripheral vascular filter from becoming dislodged from a position in a peripheral vasculature.

Abstract: A multi-laminar electrospun nanofiber scaffold for use in repairing a defect in a tissue substrate is provided. The scaffold includes a first layer formed by a first plurality of electrospun polymeric fibers, and a second layer formed by a second plurality of electrospun polymeric fibers. The second layer is combined with the first layer. A first portion of the scaffold includes a higher density of fibers than a second portion of the scaffold, and the first portion has a higher tensile strength than the second portion. The scaffold is configured to degrade via hydrolysis after at least one of a predetermined time or an environmental condition. The scaffold is configured to be applied to the tissue substrate containing the defect, and is sufficiently flexible to facilitate application of the scaffold to uneven surfaces of the tissue substrate, and to enable movement of the scaffold by the tissue substrate.

Abstract: The techniques of this disclosure generally relate to a modular stent device including a main body configured to be deployed in the ascending aorta, a bypass gate configured to be deployed in the aorta, and a bifurcated contra limb. The bifurcated contra limb includes a single proximal limb that is bifurcated (split) into a first distal limb and a second distal limb. By forming the bifurcated contra limb to include a single proximal limb that is bifurcated into the distal limbs, guiding a guide wire into the relatively larger opening of bifurcated contra limb at a proximal end is simpler than guiding a guidewire into two smaller limbs extending distally from main body. Accordingly, cannulation of the bifurcated contra limb is relatively simple thus simplifying the procedure. In addition, the parallel design mimics anatomical blood vessel bifurcations to limit flow disruptions.

Abstract: An anastomosis stent includes an elongated body of a tubular configuration having a length and diameter dimensions extending in axial and radial directions of the elongated body and in a transverse relationship to each other. The elongated body is formed by multiple rings stacked adjacent one another in a direction parallel to the length dimension. Each ring is a single strand of wire bent in a repetitive pattern of sine waves. Each sine wave defines an alternating peak and valley divided by a length dimension extending orthogonal to the length dimension of the elongated body. The rings are fused together at locations on selected pairs of adjacent peaks and valleys of the rings with the fused locations arranged in parallel rows. The elongated body includes main and end portion and a safety mark about the elongated body at the juncture therebetween.

Abstract: The present invention relates to the field of implants. In particular, the present invention relates to an implant for tissue reconstruction which comprises a scaffold structure that includes a void system for the generation of prevascularized connective tissue with void spaces for cell and/or tissue transplantation. Moreover, the present invention relates to a method of manufacturing such an implant, to the internal architecture of such an implant, to a removal tool for mechanical removal of space-occupying structures from such an implant, to a kit comprising such an implant and such a removal tool, to a removal device for the removal of superparamagnetic or ferromagnetic space-occupying structures from such an implant, as well as to a guiding device for providing feedback to a surgeon during the procedure of introducing transplantation cells into the void spaces generated upon removal of space-occupying structures from such an implant.

Abstract: Intraocular lenses that include a central portion and one or more peripheral portions. The IOLs includes a sensor housing and a communication member, both of which are secured to the central portion.

Abstract: Accommodating intraocular lenses containing a flowable media and their methods of accommodation.

Abstract: Methods for a patient surgically receiving a customized IOL for a particular eye according to patient-specific measurement data are provided. The methods may include preoperative evaluation of a particular eye of a particular patient and accumulation of patient-specific measurement data by a physician and/or a hospital. The physician, designee, and/or hospital may transmit the measurement data for the patient to the customized IOL manufacturer. The IOL manufacturer may manufacture and customize the IOL. The manufacturer may deliver the customized IOL back to the surgeon, designee, and/or hospital, after which the surgeon may perform the surgery.

Abstract: A method and system provide an ophthalmic device. The ophthalmic device includes an ophthalmic lens having anterior surface, a posterior surface and at least one diffractive structure including a plurality of zones. The at least one diffractive structure is for at least one of the anterior surface and the posterior surface. Each zone includes at least one echelette having a least one step height. The step height(s) are individually optimized for each zone. To compensate chromatic aberration of eye from distance to a range of vision, a greater than 2? phase step height may be employed and the step height(s) folded by a phase, which is an integer multiple of two multiplied by ?. Hence chromatic aberration of eye may be compensated to improve vision from distance to near.

Abstract: An assembly includes a holder device and a non-self-expandable prosthetic heart valve. The prosthetic heart valve can be radially compressed from an expanded configuration to a compressed configuration. The holder device is configured to hold the prosthetic heart valve in the expanded configuration and to allow the prosthetic heart valve to be inserted in a crimping device so that the prosthetic heart valve can be crimped onto a valve mounting portion of a delivery apparatus.

Abstract: Catheter apparatuses and methods are provided for repairing heart valves, particularly mitral valves. The method includes providing a catheter having an elongate, flexible body, with a proximal end and a distal end. The distal end can be transluminally advanced from the left atrium through the mitral valve. A distal anchor zone or portion coupled with the proximal end can extend and along the left ventricular outflow tract into the ascending aorta. A valve repair device is deployed to permanently connect leaflets at a mid-section of a mitral valve while permitting medial and lateral portions of the natural leaflets to open and close. The catheter apparatuses may be positionable using a steering device. The valve repair device detachably connects the distal and proximal ends of the catheter. The valve repair device can be detached using low profile devices actuatable from the proximal or distal ends, e.g., at a venous or arterial access site.

Abstract: A heart valve prosthesis, including a valved stent and valve leaflets, where the valve leaflets are accommodated in the valved stent, at least two valve leaflets are provided and centrosymmetrically distributed along the circumferential direction of an inner surface of the valve leaflet stent, one ends of each of two adjacent valve leaflets are combined together on the valve leaflet stent to form a valve corner, the valved stent is provided with a positioning member, and the projections of a perpendicular line of one of the valve corners to the axis of the valved stent and a perpendicular line of the positioning member to the axis of the valved stent are coincident on a plane perpendicular to the axis of the valved stent. The heart valve prosthesis can considerably reduce regurgitation at the center.

Abstract: A prosthetic heart valve includes a stent extending in a longitudinal direction and having a collapsed condition and an expanded condition. The stent includes a plurality of struts forming cells and a plurality of commissure attachment features spaced apart in an annular direction of the stent and extending in a medial direction of the stent. A valve assembly is secured to the commissure attachment features, the valve assembly including a cuff and a plurality of leaflets, each of the leaflets having a free edge and being capable of alternating between an open position and a closed position. A method of manufacturing the prosthetic heart valve is also provided.

Abstract: According to one aspect of the disclosure, a system may include a surgical prosthetic heart valve having a frame, prosthetic leaflets within the frame configured to allow blood to flow through the frame in an antegrade direction but to substantially block blood from flowing through the frame in a retrograde direction, and a cuff configured to be sutured to a native valve annulus of a heart of a patient. The system may include a valve tether having a first end configured to be coupled to the surgical prosthetic heart valve, and an anchor configured to be secured to a ventricular apex of the heart of the patient. The valve tether may include a second end opposite the first end, the second end configured to be operably coupled to the anchor.

Abstract: A method for endovascularly implanting a valve in the heart having a medical assembly including a replacement heart valve and an anchor assembly for positioning and restraining the valve. The method includes endovascularly introducing an anchor delivery system for anchoring the heart valve to replace the native heart valve and for endovascularly introducing a valve delivery systems for implanting the valve at the implantation site to replace a native heart valve.

Abstract: A prosthetic heart valve includes a collapsible and expandable stent having a proximal end and a distal end. A plurality of commissure attachment features (“CAFs”) is disposed on the stent, with each CAF including a body and a plurality of eyelets. The eyelets may be arranged in a single column or in a plurality of rows and columns. The prosthetic heart valve also includes a collapsible and expandable valve assembly including a plurality of leaflets connected to the plurality of commissure attachment features. The bodies of the CAFs may include a number of other features including, for example, a slot extending between columns of eyelets.

Abstract: Embodiments of the present disclosure provide an introducer device and method for introducing a delivery apparatus into a patient's vasculature. Disclosed methods can include positioning a sleeve of an introducer sheath in a blood vessel of a patient, the sleeve having a lattice layer with a lumen therethrough, inserting a distal end portion of the delivery apparatus and a prosthetic heart valve into the lumen, and advancing the distal end portion of the delivery apparatus through the lumen from the proximal end to the distal end. The method can then include expanding the lumen from a first diameter smaller to a second diameter at least equal to the diameter of the prosthetic heart valve to allow passage of the prosthetic heart valve through the lumen, and returning the lumen of the sleeve to a diameter smaller than the second diameter after advancing the prosthetic heart valve through the lumen.

Abstract: Apparatus and methods are described herein for use in in establishing an improved AV loop with the use of a pulley/snare device at the base of a ventricle of a heart. In some methods described herein, a pulley/snare device is established to create a path with inherent concentricity to the aortic and mitral valves, allowing the valves to function normally during an interventional procedure in the heart, without impeding the motion of any leaflets. The pulley/snare device described herein minimizes the forces that are applied on the valves or associated cardiac tissue to “make the turn” from the aortic valve to the mitral valve.

Abstract: A sequentially deployed prosthetic cardiac valve includes a self-expanding frame having an atrial skirt, a ventricular skirt, and an annular region disposed therebetween. A first anterior tab is disposed on an anterior portion of the frame. A posterior tab is on a posterior portion of the self-expanding frame. The frame may be designed so that any portion may expand sequentially in any desired order. For example, a portion of the first anterior tab and a portion of the posterior tab may partially self-expand first. Next, the first anterior tab may fully self-expand before the posterior tab fully self-expands. The posterior tab may fully self-expand next followed by the ventricular skirt, or the ventricular skirt may self-expand next followed by full expansion of the posterior tab.

Abstract: A ringless web is configured to repair heart valve function in patients suffering from degenerative mitral valve regurgitation (DMR) or functional mitral valve regurgitation (FMR). In accordance with various embodiments, a ringless web can be anchored at one or more locations below the valve plane in the ventricle, such as at a papillary muscle, and one or more locations above the valve plane, such as in the valve annulus. A tensioning mechanism connecting the ringless web to one or more of the anchors can be used to adjust a tension of the web such that web restrains the leaflet to prevent prolapse by restricting leaflet motion to the coaptation zone and/or promotes natural coaptation of the valve leaflets.

Abstract: An implantable device for penile construction includes a tissue ingrowth cover. The tissue ingrowth cover may be disposed between a penile prosthesis and an interior wall of a neophallus, when the penile prosthesis is implanted within the neophallus.

Abstract: According to one aspect of the disclosure, a method of manufacturing an implant may comprise manufacturing a first portion, coupling an insert with the first portion to form a combined first portion and insert assembly, and additively manufacturing a second portion on the assembly after the coupling step.

Abstract: The present disclosure relates to a customized medical implant for attachment to and at least partly covering the natural femoral head of a hip joint of a subject. The medical implant includes a dome shaped shell having a height h, an inner equatorial shell radius rs, an orifice radius ro, a thickness ts at the equatorial line, and a thickness tt at the top of the dome. The implant is constructed such that one or more of the thickness ts, the thickness tt, the equatorial shell radius rs, the orifice radius ro and the shell height h are customized to the hip joint of the subject based on at least one 3D computed tomography image showing substantially the entirety of the natural femoral head and the acetabulum of said hip joint.

Abstract: The invention relates to a ceramic surface arthroplasty system, which consists of a convex, hemispherical, metallic implant (1) and a hollow hemispherical metal implant (3). The implants are coated with porcelain or zirconium oxide layer on their friction surfaces to avoid the creation of metallic microparticles. The convex implant (1) has a navel (4) on the thread (6) of which a bone-piercing pre-tensioning needle (7) is screwed and is tightened with a washer (9) at the area of the major trochanter or bulge. Further, it has protruding ribs (5) immersed on the surface of the head.

Abstract: The present invention is an internal osseointegrated transfemoral amputee implant device and related methods. The device is designed to restore the enclosed nature of the bone marrow system which is disrupted by amputation, plus provide a pressure tolerant (weight-bearing) surface and mechanical anchoring for the iliotibial band.

Abstract: A total joint replacement system comprising a first and a second implant system. The first implant system includes a first implant having a first load bearing surface based on a first removed portion of an articular surface of a patient's first bone, and a first anchor having a first threaded region configured to be secured into the first bone, wherein the first anchor is configured to be secured to the first implant. The second implant system includes a second implant having a second load bearing surface based on a second removed portion of an articular surface of a patient's second bone, and a second anchor having a second threaded region configured to be secured into the second bone, wherein the second anchor is configured to be secured to the second implant.

Abstract: A joint replacement system for repairing an articular surface of a first bone of a joint includes an anchor portion and an implant portion. The anchor portion includes an anchor to be secured to the bone, and an anchor fixation head including a bone-facing surface (BFS) extending radially outward from the anchor and an implant facing surface (IFS) extending from a periphery of the BFS. The implant portion is formed from a material (e.g., CoCr) more dense than the material of the anchor portion (e.g., Ti) and includes a fixation cavity to receive at least a portion of the anchor fixation head (AFH), the fixation cavity includes an anchor facing surface (AFS) configured to form a frictional connection with the IFS, and a load bearing surface having a contour for articulating against a cooperating articulating surface of a second bone of the joint.

Abstract: The invention concerns a method for manufacturing a prosthesis (11) for a fractured long bone of a patient, the method comprising the steps of: A) providing data representative of the fractured long bone, the fractured long bone comprising a diaphyseal fragment (2) comprising a medullary cavity (8); B) based on said data, designing the prosthesis specifically to the patient, the prosthesis comprising a stem part (12) configured to be inserted into the medullary cavity, step B) comprising: a sub-step of choosing, specifically to the patient, a contact zone (40) of the medullary cavity onto which a respective chosen mechanical stress is planned to be applied by the stem part, and a sub-step of designing the stem part so that the stem part may be inserted into the medullary cavity and thus apply the chosen mechanical stress to said contact zone; and C) manufacturing the prosthesis designed at step B).

Abstract: A prosthetic glenoid implant may include a polymer bearing component, a metal base component, and a plurality of fixation members. The bearing component may have a first surface adapted to articulate with a humeral head, and an opposing second surface including a first mating feature. The base component may have a first surface and a bone-contacting surface, the first surface having a second mating feature adapted to engage the first mating feature, the bone-contacting surface adapted to contact the native glenoid. The base component may define a plurality of apertures. The fixation members may each have a head and a threaded shaft adapted to pass through a corresponding one of the plurality of apertures, the head of each fixation member adapted to be positioned within a recess defined between the base component and the bearing component in an assembled condition of the prosthetic glenoid implant.

Abstract: In one embodiment, a glenoid implant includes a body and a flange. The body includes a bearing surface and a bone-contacting surface opposite the bearing surface. The flange extends from the bone-contacting surface of the body to a free end. The flange has an inside facing surface that faces a center of the body and an outside facing surface that faces an outer perimeter of the body. The outside facing surface is opposite the inside facing surface and each of the inside and outside facing surfaces extend from the bone-contacting surface to the free end. The outside facing surface at the bone-contacting surface of the body is 8 mm or less from the outer perimeter of the body. The outside facing surface is tapered from the bone-contacting surface toward the free end. The inside facing surface is non-parallel to the outside facing surface.

Abstract: The invention relates to a prosthesis for implantation into a living body in the form of a magnetic artificial joint, in particular an artificial shoulder joint, comprising: a) a first prosthesis member comprising a socket member, b) a second prosthesis member comprising a head member, c) one of the socket member and the head member is at least partially composed as a permanent magnet and the other one of the socket member and the head member is at least partially composed of a magnetic material, or the socket member and the head member are both at least partially composed as a permanent magnet, d) the socket member comprises a recess on a surface side to be coupled with the head member, the recess comprising a concavely contoured contact surface, e) the head member comprises a projection on a surface side to be coupled with the socket member, the projection comprising a convexly contoured contact surface, f) the convexly contoured contact surface is adapted to the concavely contoured contact surface, such th

Abstract: An implant is insertable in the joint space to separate bones of the joint. The implant has two endplates each configured to engage a separate articulating bone of the joint, and a threaded member positioned between the two endplates and configured to increase the space between the two endplates when the threaded member is rotated. A rotatable gear is engaged with the threaded member, and is engageable with a rotating gear of a connected implantation tool, so that rotation of the gear on the tool causes rotation of the threaded member and expansion of the implant to separate the bones. Connector portions on the tool and the implant may be rotated together to securely engage the implant and the tool so that the gears of the tool and the implant can be rotated using an actuator outside of the body, when the implant is inside the body.

Abstract: An expandable interbody device for implantation within an intervertebral space is provided, together with methods and tools for use therewith. The interbody devices of the present invention include upper and lower bearing members configured to expand via an expansion mechanism configured to allow the insertion of osteoconductive materials and other structures into the interior of the interbody device before and after implantation, and before and after expansion of the interbody device. The insertion tool is configured expand the interbody device and to allow insertion of materials into the interbody device through a protected pathway.

Abstract: An expandable, adjustable inter-body fusion device is presented. The inter-body fusion device can have a first plate, a second plate, and an insert positioned substantially therebetween the first plate and the second plate. The first plate, the second plate, and the insert define an interior cavity. Moving the insert longitudinally with respect to the first and second plates increases or decreases the distance of the first plate with respect to the second plate, effectively expanding the inter-body fusion device and increasing the volume of the interior cavity. The angle between the first plate and the second plate is selectively adjustable.

Abstract: An implant is provided for performing spinal fusion. The implant includes an implant body having a leading side and a trailing side at opposing ends along a longitudinal axis. Between the leading side and trailing side are an upper surface, a lower surface, an anterior side, and a posterior side. At least one keel structure is provided extending from the implant body for penetration into an adjacent vertebral body. A trial sizer and keel cutter may be utilized to form keel channels within the vertebral body to receive the keel structure.

Abstract: A tool for use with an orthopaedic implant includes: a tubular assembly including a tubular passage having a first end and a second end, the first end including a means for attachment to an implant body; a plug; and a plunger coupled to the plug. The tubular passage is configured to receive, via the second end, a material agent and the plunger coupled to the plug. The plunger is configured to slide through the tubular passage for expelling the material agent from the tubular passage into a load bearing member via the at least one first opening. The plunger is configured to rotate within the tubular passage for coupling the plug with the first opening to seal the first opening against expulsion of the material agent from the load bearing member via the first opening.

Abstract: An intervertebral spacer is disclosed having a main body and an articulating component that is pivotally mounted within an opening of the main body. The intervertebral spacer is designed to be manufactured using an additive manufacturing process without the use of any frangible support material between a main body of the intervertebral spacer and an articulating component of the intervertebral spacer. To this end, an article of manufacture is provided in which supports are formed prior to forming intervertebral spacer. The supports are configured to support the main body and the articulating component such that they can be separately, but simultaneously manufactured using an additive manufacturing process atop the supports, without the need for any frangible support material therebetween.