Various aspects of the present disclosure are directed toward apparatuses, systems, and methods that include a cord that is flexible and elongated defining a length. The cord may include a core having a porous surface and a porosity-reducing element on at least a portion of the core.

A system comprising a biomimetic electrochemical eye (EC-EYE) and a computing device is provided. The EC-EYE comprises: an ionic liquid device; a nanowire (NW) device that comprises the plurality of NWs; and a connection device configured to provide a plurality of currents associated with the plurality of NWs to a computing device. The computing device comprises one or more processors and a display device. The one or more processors are configured to: receive the plurality of currents from the plurality of NWs via the connection device; determine a plurality of pixel characteristics associated with a plurality of pixels based on the plurality of currents from the plurality of NWs; generate an image comprising the plurality of pixels based on the plurality of pixel characteristics; and provide the image to a display device. The display device is configured to display the image.

Various embodiments disclosed relate to contact lens including nanopores. A contact lens can include a nanoporous film including nanopores that are on an inner surface of the contact lens, and a backing lens on the nanoporous film. Various embodiments further include a biomarker-sensing region of the nanoporous film, a drug storage and delivery region of the nanoporous film, or a combination thereof.

A corneal implant (10) includes a central portion (12) and a peripheral skirt (14) extending outwards from the central portion (12), and at least a portion of the peripheral skirt (14) includes a mesh (16).

Various aspects of the present disclosure are directed toward an embolic filter system. The embolic filter system generally includes a filter and an elongated element. In some examples, the elongate element extends to a position distal to a proximal end of the filter and operates to protect against medical devices entangling with the filter. In some examples, the elongate element is soft and compliant and operates with a hemostatic seal to provide for a hemostatic seal within a lumen of the elongate element while maintaining the lumen as a working lumen through which medical devices can be passed.

Provided herein are implantable devices, such as vascular grafts and access port for hemodialysis, that include a microporous sheath layer having a corrugated outer surface, and use therefore for reducing the risk of infection or stenosis.

An apparatus is provided for draining aqueous humor from an eye for reducing intraocular pressure. The draining apparatus comprises a tube defining a passage for fluid flow between an inlet end and an outlet end. An outlet assembly contacts the conjunctival layer externally of the eyeball. The outlet assembly comprises a housing in fluid communication with the outlet end of the tube and having an aperture for allowing egress of aqueous humor onto the external ocular surface. A resistive component is disposed in the housing for providing resistance to a flow of aqueous humor. A pair of tabs project outwardly and are adapted to be disposed subconjunctivally for securing the draining apparatus relative to the eyeball.

Some implementations of an endovascular device include a stent graft with an expandable tubular metallic frame and a covering material disposed on at least a portion of the metallic frame. The stent graft defines a lumen therethrough. In a particular embodiment, a first balloon is disposed around an outer periphery of the stent graft, a second balloon is disposed around the outer periphery of the stent graft and spaced apart from the first balloon, and a third balloon is disposed within the stent graft lumen between the first balloon and the second balloon. The third balloon can be inflated to fully or partially occlude the lumen. The first and second balloons can be individually inflated to fully or partially shunt blood flow from a blood vessel through the stent graft. In some embodiments, sensors and an automated control unit are included to automate the operations of the endovascular device.

A stent with a selectively covered end region. The stent includes a radially expandable tubular framework and a covering surrounding the tubular framework. The covering includes a skirt surrounding a distal end region of the tubular framework which is selectively removable from the distal end region of the tubular framework to expose the distal end region of the tubular framework to permit hyperplastic tissue ingrowth through the distal end region of the tubular framework. For example, the skirt may be folded, rolled, collapsed, or separated from the remainder of the covering to expose the distal end region of the tubular framework.

A surgical implant device may include a first substantially planar portion having a first surface area, a second substantially planar portion having a second surface area, and a coupling device for connecting the first substantially planar portion to the second substantially planar portion. The coupling device facilitates expanding and contracting the first and the second substantially planar portion in order to provide an implant surface area corresponding to the first surface area during insertion of the surgical implant within an incision, and having a third surface area corresponding to both the first surface area and at least a portion of the second surface area following insertion of the surgical implant within the incision.