Abstract: An accommodating intraocular lens (AIOL) for implantation within a capsular bag of a patient's eye comprises first and second components coupled together to define an inner fluid chamber and an outer fluid reservoir. The inner region of the AIOL provides optical power with one or more of the shaped fluid within the inner fluid chamber or the shape of the first or second components. The fluid reservoir comprises a bellows region with fold(s) extending circumferentially around an optical axis of the eye. The bellows engages the lens capsule, and a compliant fold region between inner and outer bellows portions allows the profile of the AIOL to deflect when the eye accommodates for near vision. Fluid transfers between the inner fluid chamber and the outer fluid reservoir to provide optical power changes. A third lens component coupled to the first or second component provides additional optical power.

Abstract: To provide a bioabsorbable stent including: a first tubular unit containing a plurality of cells coupled to each other, each of the cells formed from substantially linear parts and a substantially circular arc part and having a substantially U shape which opens to one end in the axial direction of the stent; and a second tubular unit having the same shape as that of the first tubular unit, the second tubular unit containing a plurality of cells each of which has a substantially U shape which opens to a direction opposite to the opening direction of the opposing first cell. The first tubular unit and the second tubular unit are alternately arranged in sequence to surround a central axis of the stent. Coupling members couple substantially linear parts in some of the opposing cells in the respective neighboring tubular units.

Abstract: Disclosed is an intraocular lens (IOL) including an anterior surface, a posterior surface and an optical axis. At least one of the anterior or posterior surfaces has a diffractive profile formed thereon. The diffractive profile has diffractive focal points for far vision, intermediate vision, and near vision. The diffractive profile corresponds to a superposition of a first partial diffractive profile and a second partial diffractive profile, the first partial diffractive profile has a focal point of order +n that coincides with the diffractive focal point for intermediate vision or with the diffractive focal point for near vision, the second partial diffractive profile has a focal point of order +n that coincides with the diffractive focal point for far vision and a focal point of higher order than +n that coincides with the diffractive focal point for near vision.

Abstract: An optical device (2300) including a partial or incomplete optic (2320) configured operatively as an add-on (e.g., supplemental lens/optic) for an (existing) optical element or system, the partial or incomplete optic having an active area configured in relation to the optical element or system such that the partial or incomplete optic controls or changes foci of light incident upon or provided to the active area, but does not control or change foci of light bypassing optically relevant portions of the partial or incomplete optic, and associated methods for enhancing vision.

Abstract: An ophthalmic device includes an optic including an optic axis and an open-loop haptic structure coupled with the optic. The open-loop haptic structure includes a pair of open loops, the pair of open loops comprising a first open loop and a second open loop. At least a portion of the first open loop extends in a first angular direction. At least a portion of the second open loop extends in a second angular direction, the second angular direction being opposite the first angular direction.

Abstract: A breast shaping method using a barbed suture and a suture handling device. The breast shaping method includes inserting a tensioning barbed suture in medialmost and lateralmost portion of the inframammary fold from deep soft tissues (muscle/pericondrium-periostium to and along the subdermal layer of the inframammary fold, with an end portion of the barbed suture being left outside of the skin, thereby allowing the barbed suture to be tensioned, tensioning the end portion of the barbed suture arranged by the insertion of the barbed suture, so that the barbed suture pulls tissues of the subdermal layer, thereby lifting the inframammary fold and defining a nice indentation of the inframammary fold, and cutting the end portion of the barbed suture outside of the skin after the tensioning of the barbed suture.

Abstract: A liner for a prosthesis, wherein the liner is made of a liner material and comprises a proximal opening for accommodating an amputation stump, a distal end, a longitudinal direction, which extends from the proximal opening to the distal end, and an auxetic material The auxetic material is a two-dimensional-auxetic material, which is arranged in such a way that an extension of the liner in the longitudinal direction leads to an expansion of a diameter of the liner.

Abstract: Mitral valve prolapse and mitral regurgitation can be treating by implanting in the mitral annulus a transvalvular intraannular band. The band is positioned so that it extends transversely across a coaptive edge formed by the closure of the mitral valve leaflets, to inhibit prolapse into the left atrium. At least one marginal chordae is severed, to permit leaflet closure against the band.

Abstract: An ophthalmic apparatus includes a support structure; a substrate included with the support structure; at least one conductor disposed on the substrate; and a hermetic barrier structure disposed over the at least one conductor. The hermetic barrier structure further includes a stack of alternating flexible insulating material and superelastic metal alloy layers.

Abstract: The present invention includes a device for effecting deformation of a sclera of an eye, including an expandable, mesh tube having holes dispersed through an entire surface thereof and with first and second tapered ends, and inserted unexpanded to deform the sclera when expanded. A central portion is intrascleral, with the first and second tapered ends external to the sclera on top of an intact scleral surface to deform during expansion, and simultaneously causes the sclera to be deformed so that the sclera moves towards the inside of the eye while simultaneously causing the sclera to move towards the outside of the eye. The mesh tube includes struts, connecting points of the struts are of different sizes, the first and second tapered ends and the connecting points within the tapered ends are thicker than the connecting points of the mesh tube, and the mesh tube includes fixation tabs.

Abstract: A lower limb exoskeleton system includes a back frame, hip joint movement mechanisms, telescopic thigh bars, knee joint movement mechanisms, shank bars, foot jump-down cushioning mechanisms, a waist binding frame, upper leg binding frames and lower leg binding frames. Two protruding ends of the back frame are connected with a top end of each of the telescopic thigh bars respectively via the hip joint movement mechanisms, bottom ends of the telescopic thigh bars are connected with a top end of the corresponding shank bars respectively via the knee joint movement mechanisms, and bottom ends of the shank bars are connected with the foot jump-down cushioning mechanisms. The waist binding frame is arranged on an inner side of a horizontal part of the back frame, and the upper leg binding frames and the lower leg binding frames are arranged on the telescopic thigh bars and the shank bars respectively.

Abstract: A method of implanting a prosthetic stemless shoulder implant may include making an incision into a patient's shoulder area of a patient and passing a cutting instrument through a rotator cuff interval of the patient. A central portion of the native humeral head may be resected and removed so that a central void remains. The same or another cutting instrument may be inserted through the rotator cuff interval and into the central void. Medial and lateral portions of the native humeral head adjacent the central void may be resected and removed. A base of a prosthesis may be implanted into a proximal portion of the humerus after passing the base through the rotator cuff interval, and two humeral head portions may be inserted through the rotator cuff interval and coupled to the base and to one another.

Abstract: A prosthetic adaptor includes a post plate, a grip plate coupled to the post plate, and an equipment interface coupled to the post plate. The equipment interface can be coupled to the post plate at an end of the post plate distal from the grip plate. The post plate can include a concave surface. The concave surface can be configured to receive a Hosmer-like prosthetic hook.

Abstract: An endovascular heart valve assembly includes an inner frame comprising a graft covering housing a prosthetic heart valve, an outer frame formed from a metallic material and defining a gridded configuration. A sealing material includes a plurality of radially extending fibers that extend outwardly of the outer frame. The plurality of radially extending fibers include first fibers extending from a first position relative to the outer frame and second fibers extending from a second position relative to the outer frame that is distally spaced-apart from the first position. The gridded configuration includes an uncovered open cell between the first position and the second position. The first fibers and the second fibers are configured to cooperatively form a seal when compressed within the aortic annulus. A length of the first fibers is greater than a height of the uncovered open cell.

Abstract: Anchor devices and methods can be used to secure a prosthetic valve to a native valve annulus. The anchor device can be a separate expandable element from the prosthetic valve that is first advanced to the annulus and deployed, after which an expandable prosthetic valve is advanced to within the annulus and deployed. The combination of the two elements can apply a clamping force to the valve leaflets which holds the prosthetic valve in place. The anchor device can have a lower or ventricular portion and an upper or atrial portion. The anchor device can include one or more leaflet clamping portions. One, two, or more upstanding vertical posts between the clamping portions can extend upward at the valve commissures and support the upper portion, which can include one or more structures for leak prevention.

Abstract: A stentless support structure capable of being at least partly assembled in situ. The support structure comprises a braided tube that is very flexible and, when elongated, becomes very long and very small in diameter, thereby being capable of placement within a small diameter catheter. The support structure is preferably constructed of one or more thin strands of a super-elastic or shape memory material such as Nitinol. When released from the catheter, the support structure folds itself into a longitudinally compact configuration. The support structure thus gains significant strength as the number of folds increase. This radial strength obviates the need for a support stent. The support structure may include attachment points for a prosthetic valve.

Abstract: An endovascularly deployed prosthetic includes a portion for being positioned within an ascending aorta. The prosthesis includes a replacement aortic valve on a proximal end thereof. The prosthesis includes an increased diameter portion that seals against the aorta at a more distal portion, and a pair of conduits extend from the increased diameter portion to the coronaries for fluidly coupling the coronaries to the prosthesis.

Abstract: Mitral valve prolapse and mitral regurgitation can be treating by implanting in the mitral annulus a transvalvular intraannular band. The band has a first end, a first anchoring portion located proximate the first end, a second end, a second anchoring portion located proximate the second end, and a central portion. The central portion is positioned so that it extends transversely across a coaptive edge formed by the closure of the mitral valve leaflets. The band may be implanted via translumenal access or via thoracotomy.

Abstract: Knowledge of the anatomical, post-operative position and orientation influences not only the selection of the IOL to be implanted but also the result of the refractive operation on the eye. In the method for selecting an IOL to be implanted into an eye on the basis of the prediction of the anatomical, post-operative position (ALP) and orientation thereof, based on pre-operative measuring values such as, for example, anterior chamber depth (VKT), lens thickness (LD) and axial eye length (AL), the invention additionally or exclusively uses the curvature(s) of the eye lens or measuring values derived therefrom. The proposed method is used to predict the anatomical, post-operative position (ALP) and orientation of an intraocular lens (IOL) to be implanted into an eye.

Abstract: A transcatheter aortic valve replacement (TAVR) device includes a paravalvular seal that includes outwardly extending fibers that create a seal with the aortic annulus when the TAVR is deployed.