Abstract: A bifurcated endovascular prosthesis that includes a tubular main body having a diameter, a proximal end, a distal end, an internal lumen extending from the proximal end to the distal end, an anterior side, and a posterior side. The anterior and posterior sides are opposite each other circumferentially around the internal lumen. The prosthesis also includes a first limb that extends from the distal end of the tubular main body along the anterior side of the main body. The first limb has a diameter less than the diameter of the tubular main body and having a proximal end and a distal end. The prosthesis also includes a fenestration adjacent to the proximal end of the first limb. The fenestration extends from the proximal end of the first limb to the posterior side of the tubular main body. The prosthesis also includes a second limb that extends within the internal lumen from the fenestration toward the proximal end of the tubular main body.

Abstract: A transcatheter prosthesis with radially compressed and expanded configurations. An elongate member encircling at least a portion of the prosthesis, and configured to provide a seal between the prosthesis and a native anatomy when the prosthesis is deployed in the radially expanded configuration. The elongate member may be a resilient elongate member having a radially contracted state, when in tension, to hold at least the portion of the prosthesis in the radially compressed configuration, and having a radially expanded state, when relaxed, to provide the seal between at least the portion of the prosthesis and a native anatomy when the prosthesis is deployed. A system for delivering the transcatheter prosthesis may include a delivery catheter having an elongate cinching member encircling at least a second portion of the prosthesis, wherein the elongate cinching member is configured to hold the second portion of the prosthesis in the radially compressed configuration.

Abstract: A heart valve prosthesis is proposed, including a housing, at least one leaflet installed within the housing, at least one sensor and/or valve performance monitoring device. The sensor and/or monitoring device is built into the housing and/or leaflet. In an embodiment, the housing and/or leaflet has an oscillating circuit including an inductor coil connected to the sensor and/or monitoring device. One such coil can be built into the housing, and another coil can be built into the leaflet. In another embodiment, one coil can be built into a first leaflet, and another coil can be built into a second leaflet, wherein the sensor and/or monitoring device determines a degree of opening/closing the leaflets by measuring inductive interconnection between the coils, and operation timing characteristics of the valve. In an embodiment, the valve may include an emission sensor disposed within the leaflet and/or housing capable of detecting the valve's open/closed positions.

Abstract: An intraocular lens includes an annular housing coupled to a first window to form a lensing cavity. Disposed within the lensing cavity is two immiscible liquids, including a first liquid and a second liquid which form a meniscus at an immiscibility interface between the first liquid and the second liquid within the lensing cavity. The intraocular lens includes a flexible reservoir to store a variable portion of the first liquid. The flexible reservoir is disposed about at least a portion of a periphery of the annular housing. The intraocular lens also includes at least one channel linking the flexible reservoir to the lensing cavity to permit a transfer of the first liquid between the flexible reservoir and the lensing cavity. The transfer of the first liquid changes a curvature of the meniscus to adjust optical power of the intraocular lens.

Abstract: An accommodating intraocular lens assembly can include a first lens, a first plurality of stanchions, a second lens, and a second plurality of stanchions. A central optic axis can extend through centers of the first and second lenses. The first plurality of stanchions can each extend a first distance between a first base end and a first distal end. The first lens can be connected with the first distal ends. The second plurality of stanchions can each extend a second distance between a second base end and a second distal end. The second lens can be connected with the second distal ends. Compression at the peripheries of the stanchions induces movement of the lenses apart from one other.

Abstract: A stent is provided having a plurality of intersecting elongated members arranged to form a plurality of cells, which define an elongated tube with a lumen. The elongated tube has first and second sections, the first section having a substantially constant first diameter, the second section having a substantially constant second diameter that is larger than the first diameter. The elongated tube also has a transition section between the first and second sections, the transition section having a concave curvature extending proximally from the first section and a convex curvature extending proximally from the concave curvature to the second portion. A proximal end of the second section has a plurality of rounded ends formed by the plurality of intersecting elongated members. Each of the plurality of cells within the first section have a pitch that is tighter than each of the plurality of cells within the second section.

Abstract: A stent is provided having a plurality of intersecting elongated members arranged to form a plurality of cells, the plurality of cells defining an elongated tube with a lumen running therethrough. The elongated tube has first, second, and third sections, the first section having a substantially first diameter and the third section having a substantially constant second diameter that is larger than the substantially constant first diameter of the first section, wherein the diameter of the second section transitions from the first diameter to the second diameter. Each of the plurality of cells within the first section have a pitch that is tighter than each of the plurality of cells within the second and third sections. In the second section, the plurality of intersecting elongated members includes a plurality of pairs of elongated members, wherein each pair of elongated members includes two adjacent elongated members twisted axially around each other.

Abstract: The present technology is a prosthetic heart valve device, and related systems and methods, for treating a native valve of a human heart having a native annulus and native leaflets. One embodiment comprises a valve support having an inflow region and an outflow region, and a prosthetic valve assembly within the valve support. The device further includes an anchoring member having a base attached to the outflow region of the valve support, a plurality of arms projecting laterally outward from the base and inclined in an upstream direction in a deployed state, and a fixation structure extending upstream from the arms. The fixation structure has a plurality of struts that define an annular engagement surface configured to press outwardly against the native annulus and a plurality of fixation elements projecting from the struts.

Abstract: Adjustable vision modification using various systems, devices, and processes are provided. Adjustable vision modification may include sensing ocular related physiological activities of a user and making adjustments in an ocular device or ocular system to change the vision of the user. Various sensors and sensor locations may be employed in embodiments to sense or otherwise obtain these physiological activities. Likewise, various ocular devices, ocular processes, and ocular systems may be employed for improving vision.

Abstract: An intra ocular lens (IOL) for placement in the capsular bag and securing the IOL in an opening in an anterior part of a capsular bag, with an anterior capsular bag flap surrounding said opening. An anterior side, which in use when the IOL is implanted in an eye is directed towards a cornea of the eye. A posterior side, which in use when the IOL is implanted in an eye is directed towards a retina of the eye. The IOL comprises an optical structure, at least two posterior supports to provide support for a posterior surface of an anterior capsular bag flap, and at least two anterior supports to provide support for an anterior surface of an anterior capsular bag flap, when IOL residing inside and outside of the anterior capsular bag flap respectively.

Abstract: The present disclosure is directed to a branched endoprosthesis comprising a graft component and at least one support component. In various embodiments, the branched endoprosthesis comprises a body portion and a plurality of leg portions, wherein the legs are in an aligned configuration for ease of cannulation. In various embodiments, at least one leg is in an open configuration for ease of cannulation. Cannulation methods are also described.

Abstract: Provided is a medical base material that is suitable for regeneration of a cardiovascular system being exposed to high pressure from a lumen, such as an aorta and is absorbed by a living body after transplantation. The medical base material of the present invention has a sheet shape, a tube shape, or a combined shape thereof and is used for regeneration of a cardiovascular system by being transplanted in a body. The medical base material has a multilayer structure at least including an inner layer to be arranged on the intimal side of the cardiovascular system and an outer layer to be arranged on the adventitial side of the cardiovascular system from the inner layer and made from a material at least including a stereo complex polylactic acid. The layer to be arranged on the adventitial side of the cardiovascular system from the inner layer is formed in a porous form such that a nutrient blood vessel reaches the inner layer or enters the vicinity of the inner layer.

Abstract: A hybrid modular endovascular graft wherein a main graft is sized to span at least a portion of a target vessel lesion in a large percentage of patients. Graft extensions may be secured to the main graft to extend the main graft and provide a sealing function for some applications.

Abstract: A hair implant suitable for subcutaneous implantation is provided having an anchor comprising an anchor body, and at least one collagen receiving structure selected from the group consisting of at least one tunnel disposed through the anchor body and an external surface feature of the anchor body. The anchor further comprises at least one hair strand projecting from a distal end of the anchor body, wherein the at least one collagen receiving structure is configured to support collagen ligature growth after subcutaneous implantation of the hair implant so as to anchor the anchor to a hair implant recipient, and the collagen receiving structure is free of hair.

Abstract: A method and system provide an ophthalmic device including an optic and a haptic. The optic includes at least one optical material having a first Young's modulus. The haptic is coupled with the optic. The haptic includes at least a second Young's modulus greater than the first Young's modulus and less than 1.8 GPa. Thus, the haptic is stiffer than the optic, but more flexible than a material such as polymethyl metacrylate (PMMA).

Abstract: 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.

Abstract: A tonic ophthalmic lens is described in which refractivity of the lens differs between a first direction on a plane perpendicular to an optical axis of the lens and a second direction which differs from the first direction on the plane. In addition, refractivity difference which is the difference between the refractivity in the first direction and the refractivity in the second direction varies depending on a position of the lens in a radial direction.

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: A prosthetic heart valve for replacing a native valve includes a stent extending between an inflow end and an outflow end, and a valve assembly disposed within the stent. The prosthetic heart valve may include a supra-annular feature configured to anchor and seal the prosthetic valve above the native valve annulus and a sub-annular feature configured to anchor and seal the prosthetic valve below the native valve annulus. Each of the sub-annular feature and the supra-annular feature may be a sealing ring or a strut that extends radially outward from the stent. The prosthetic heart valve may be implanted in the patient via a sutureless approach and provide anchoring in a variety of patient populations, including those with resected native valve leaflets.

Abstract: A intraocular lens system includes an artificial capsular bag adapted for implantation within a natural capsular bag of an eye and an intraocular lens adapted to be received within the artificial capsular bag. At least a portion of the intraocular lens tilts and moves forwards within the artificial capsular bag under gravitational force with respect to a cornea and retina of the eye to create myopia.