The present disclosure, in certain embodiments, relates to a flexible and non-absorbent vaginal insert device that is easier to insert and remove and is for use in improving and preventing symptoms associated with pelvic organ prolapse and urinary and/or fecal incontinence when the device is inserted. In certain embodiments, the device has an optionally cone-shaped upper portion that provides pelvic organ support and a removal portion or stem that facilitates insertion and removal of the device.

Methods for the rapid retraction of trans-catheter heart valve delivery systems are provided. A rapid retraction trans-catheter heart valve delivery system comprises a catheter based delivery system. The delivery system has internal mechanisms that allow for the controlled deployment of a heart valve prosthesis, as well as mechanisms that allow for quickly closing the catheter once the heart valve prosthesis has been implanted. This rapid retraction ability allows for reduced procedural durations and thus reduced risk to the patient.

In implementations of systems for management of dry eye syndrome, a palpebral fissure width is determined as a distance between a medial canthus and a lateral canthus of closed eyelids. An ideal eyelash length is generated based on the distance. Prostheses having the ideal eyelash length are attached to candidate eyelashes of an upper eyelid of the closed eyelids. The prostheses introduce a turbulence to airflow around a tear film which prevents the tear film from evaporating. Dry eye syndrome is managed by preventing the tear film from evaporating.

Implant includes a body and a utile feature, for example, a smooth articulating surface. A transverse rail stem system with a plurality of rails is provided, spaced apart from the utile feature, which is adapted for transverse insertion into a bodily substrate, for example, resected bone. A surgical templatefor example, to assist in sawing, drilling with a drill bit and drill guide, and broaching with a broachalong with such bone removal tools can help prepare the bone for receipt of the implant.

Arthroplasty components include an articular surface and a bone-facing surface. The bone-facing surface includes a concave arrangement of planar surfaces which converge as they approach a middle portion of the articular surface. Instruments and implantation methods are also disclosed.

Techniques and systems for distracting a spinal disc space and supporting adjacent vertebrae are provided. Trial instruments are insertable into the disc space to determine a desired disc space height and to select a corresponding implant. Implants can be also be self-distracting and the implant providing the desired disc space height can be implanted in the spinal disc space.

The invention relates to a device for treating a native valve comprising a body having two elongated segments, each elongated segment having a connecting end, both connecting ends being able to be bound to each other, and a traction end, the traction end including an attachment element for attachment to a traction system. Each traction end comprises a locking element.

An apparatus for repairing the function of a diseased valve includes a tubular first support member which is expandable to a first average diameter and has oppositely disposed proximal and distal first support member ends. A tubular second support member is spaced axially apart from the first support member and is expandable to a second average diameter that is smaller than the first average diameter. The second support member has oppositely disposed proximal and distal second support member ends. A tubular graft section interconnects the first and second support members and has oppositely disposed proximal and distal graft section ends axially spaced apart by a graft section body. The proximal graft section end is connected directly to the distal first support member end and the distal graft section end is connected directly to the proximal second support member end.

The present application relates to novel intraocular devices and their use in surgical techniques, as well as the novel surgical methodology achieved from their use.

A stent graft system includes a plurality of stents that are configured to be assembled in situ to provide an aortal stent graft assembly. The system may include a tubular segment that is configured to engage healthy aortic tissue, a plurality of segments configured to sealingly engage the tubular segment and comprising one or a plurality of vents or side channels that are oriented proximally and are configured to receive and seal with smaller-diameter stent grafts. In some embodiments, the system further includes a tubular segment having a bifurcated distal end. For example, the system may be assembled to provide a flow channel and support structure for stent grafts that engage one or more of the right and left iliac arteries, the celiac artery, the superior mesenteric artery, and the renal arteries.