The technology disclosed herein generally concerns a system and method for reversibly occluding a body lumen.

A stent for insertion into a vessel of a patient includes an inner tube comprising a positive Poisson's ratio (PPR) material and defining a lumen extending along a longitudinal axis of the stent; and an outer tube comprising a negative Poisson's ratio (NPR) foam material and disposed around an entirety of the inner tube, the outer tube extending along the longitudinal axis of the stent. The stent is configured to exhibit an auxetic behavior in response to a deformation of the stent. An outer surface of the second portion is configured to apply a pressure to an inner surface of the vessel when the stent is implanted into the vessel and the deformation is removed.

The present invention relates to a TIPS stent graft, comprising a tubular component having a lumen extending therethrough, the tubular component comprising a balloon expandable central section and a first and a second self-expanding section, the first and the second self-expanding section sandwiching the central section, the lumen extending through the first, central, and second sections, the stent graft being capable of selectively constricting the central section.

The present technology is directed to the treatment of cardiac valves. Many embodiments of the present technology comprise an anchor member configured to be positioned at an implantation site proximate a native valve annulus. The anchor member may comprise an expandable structure having a first portion and a second portion. When the first portion is positioned at the implantation site at body temperature and released from a constrained delivery state, the first portion is configured to self-expand into apposition with tissue at or near the annulus to secure the anchor member at the implantation site. The second portion remains in a low-profile state at or around body temperature and is configured to expand into apposition with tissue at or near the annulus when heated above a second temperature greater than the first temperature and body temperature.

Devices are provided with an internal dimension that can be reduced and increased in vivo. In one example, an interatrial shunt for placement at an atrial septum of a patient’s heart includes a body. The body includes first and second regions coupled in fluid communication by a neck region. The body includes a shape-memory material. The body defines a passageway through the neck region for blood to flow between a first atrium and a second atrium. The first and second regions are superelastic at body temperature, and the neck region is malleable at body temperature. A flow area of the passageway through the neck region may be adjusted in vivo.

A retrievable medical stent is disclosed herein. The stent may include a substantially cylindrical configuration defining a longitudinal axis, an open proximal end, an open distal end, a stent lumen extending therebetween, and a contracting member circumscribing at least one of the open proximal end or the open distal end.

The disclosure describes an annuloplasty device that includes a wire configured to extend around at least part of an annulus of a cardiac or vascular valve, such as at least partially around a circumference of the annulus, and a plurality of anchors. The anchors of the plurality of anchors are configured to engage the wire and anchor the wire to the annulus. The wire is configured to urge at least some anchors of the plurality of anchors toward each other in a radially inward direction to decrease a distance between valve leaflets that extend from the annulus.

The invention relates to an implant for implanting in and/or an eye using fixing means enabling improved fixing, in particular with respect to the natural variability of the anatomical conditions of the eye. According to the invention, the fixing means comprise at least one support element which can be mounted on a tissue structure in the direction traverse to the optical axis of the eye.

An embodiment includes a process for treating an abdominal aortic aneurysm (AAA) endoleak with a shape memory polymer (SMP) foam device. First, a bifurcated stent graft is placed within the aneurysm while a micro guidewire is positioned within the aneurysm for future catheter access. Second, after placing the iliac graft extension, a catheter is introduced over wire to deliver embolic foams. Third, embolic foams expand and conform to the aneurysm wall. Fourth, embolic foams create a stable thrombus to prevent endoleak formation by isolating peripheral vessels from the aneurysm volume.

Novel intraocular lenses comprising at least one haptic having a shape memory alloy with a transition temperature substantially higher than the human body temperature, the shape memory alloy being post-surgically, selectively adjustable with a laser beam.