A replacement mitral valve prosthesis includes a support structure and a valve body having three flexible leaflets. The support structure preferably includes an internal valve frame and an external sealing frame. The valve frame supports the flexible leaflets. The sealing frame is adapted to conform to the shape of the native mitral valve annulus. The sealing frame may be coupled to an inlet end of the valve frame, an outlet end of the valve frame, or both. A plurality of anchors is coupled to the outlet end of the valve frame. The anchors extend radially outwardly for placement behind native leaflets. The prosthesis preferably includes a skirt disposed along an exterior of the external sealing frame. The prosthesis is collapsible for delivery into the heart via a delivery catheter. The prosthesis is configured to self-expand for deployment in the heart when released from the delivery catheter.

An earpiece is provided. The earpiece can deform flexibly so as to follow the earhole when in use, and the earpiece can be manufactured easily. An earpiece includes an earpiece body and a filler filled in the earpiece body. The earpiece body has a container-like base member formed of a rubber-like elastic diaphragm that is shaped like a container and has an opening portion. The earpiece body also has a lid member that seals the opening portion liquid-tightly. The filler is flowable at room temperature.

A surgical prosthetic heart valve has a supporting structure and a plurality of leaflets, the supporting structure generally having an annular shape with a blood flow channel defined in the annular shape and having opposite inflow and outflow sides along an axial direction of the annular shape, the plurality of leaflets connected to the supporting structure to control the blood flow channel to open or close. The supporting structure includes a first annular band and a second annular band, both of which are provided with deformable sections spaced from each other in the circumferential direction for allowing diameter expansion of the respective annular bands. The surgical heart valve achieves the diameter expansion of the annular bands through the deformable sections, thereby addressing the problem of postoperative variation in a valve-in-valve operations.

Intraocular implants and methods of making intraocular implants are provided. The intraocular implant can include a lens body having a lens material and a mask having a mask material. The lens body can be secured to the mask. The mask material can include a modulus of elasticity that is greater than or equal to a modulus of elasticity of the lens material.

Devices, systems, and methods for implanting a patient-specific prosthesis at a treatment site in a patient are disclosed herein. In some embodiments, a patient-specific prosthesis includes a tubular graft and a coupling member. A fenestration can be disposed in the tubular graft, the fenestration corresponding to a predicted branch blood vessel location. The coupling member can be disposed about the fenestration. The coupling member can include a coil configured to expand from a first configuration to a second configuration in response to the application of an expanding force. The coil can be configured to contract to a third configuration upon removal of the expanding force.

The invention is generally related to an intervertebral implant for replacing an intervertebral disc of the human spine. The intervertebral implant includes a first conformable endplate, the first conformable endplate being conformable to a boney vertebral endplate under an anatomical load, a second endplate and a core between the endplates, wherein the first conformable endplate partitions the core from the boney vertebral endplate, whereby the core does not contact the boney vertebral endplate. The invention is also directed to a method of replacing an intervertebral disc. The method includes removing at least a portion of an intervertebral disc to form an intervertebral disc space, implanting a first conformable endplate, into the intervertebral disc space and in contact with a first boney vertebral endplate, the first conformable endplate being conformable to the first boney vertebral endplate under an anatomical load; implanting a second endplate into the intervertebral disc space and in contact with a second boney vertebral endplate; and implanting a core between the first conformable endplate and the second endplate, wherein the first conformable endplate partitions the core from the first boney vertebral endplate, whereby the core does not contact the first boney vertebral endplate.

Reversibly deformable corneal implants for replacing excised corneal tissue, the implants including an optical portion and an anchoring portion having different mechanical properties from each other.

An apparatus for repairing or replacing a mitral valve and a method of using same are disclosed. The apparatus has an atrial band securable to a ring-shaped ventricular band. The ventricular band has an anterior band and a posterior band connectable to the anterior band. The atrial and anterior bands each have a pair of apertures. Each of the apertures is positioned proximate to a respective terminal end of the bands. The apertures of the atrial and anterior bands are arranged to align with one another when their inner surfaces engage. Means are provided to secure the atrial band to the anterior band. When delivered and implanted, the apparatus is arranged to extend across the commissures of the heart, with atrial and anterior bands arranged to press against the atrial and ventricular surfaces of the mitral valve leaflets respectively.

A blood conduit with stent has a flexible conduit body and an expandable stent structure. The conduit body has a first opening end through which only an inflow of a blood enters and a second opening end through which only an outflow of the blood leaves. The stent structure includes a plurality of threads adhered to the conduit body and expands in directions intersecting an axial direction of the conduit body. A boundary of one of the threads of the stent structure closest to the second opening end is away from the second opening end with a predetermined distance, thereby preventing blood back flow into the false lumen via a new tear.

A radially expandable, tubular stent, includes a first section having a first crush resistance force and a second section have a second crush resistance force, wherein the first crush resistance force is less than the second crush resistance force. The first section is connected to the second section to form a tube, connection of the first and second sections extending in an axial direction of the tube.