Methods for the diagnosis and treatment of nonstenotic carotid plaques and symptomatic nonstenotic carotid disease (SyNC) are described. In particular, methods of evaluating the presence of unstable plaque/thrombus and methods of treatment that include deploying plaque stabilizers (PSs) into the cerebral vasculature are described. The invention further describes plaque stabilizers, uses of plaque stabilizers and plaque stabilizer kits.

An implant material having an implant surface comprising a plurality of tissue-contacting members arranged in a regular or irregular two-dimensional array, each tissue-contacting member having a convex curved tissue-contacting surface. Methods of preparing and using such implant materials.

An aortic stent graft includes a stent with a framework attached to a fabric tube by a plurality of suture ties. The fabric tube includes a plurality of discrete attachment areas that are at least partially surrounded by at least one permeable graft area. The fabric tube is one of a weave and a knit of thermoplastic yarn. Each of the suture ties associated with the discrete attachment areas at least one of penetrates through and encircles a respective one of the discrete attachment areas. The weave or knit of the discrete attachment areas is identical to that of the permeable graft area with an exception that a wall thickness of each of the discrete attachment areas is flattened relative to, and thinner than, a wall thickness of the permeable graft area.

The invention relates to an artificial eye lens comprising an optical part, which has a first optical side as viewed in a direction of an optical principal axis of the artificial eye lens and an opposite second optical side, wherein a structure with at least one depression is formed in a haptic arrangement of the artificial eye lens and/or in a surround that surrounds the optical part at least in certain areas and that differs from the haptic arrangement, wherein the structure is formed as a micro-perforation with a multiplicity of perforation zones and at least some perforation zones are filled at least in certain areas with at least one medicament for the purposes of producing a medicament repository. The invention also relates to a method for producing such an artificial eye lens.

The invention relates to endovascular medical implant devices and materials of composition for forming these devices to provide improved mechanical properties and biodegradability. The devices include a combination or integration of superelastic material, biodegradable metal and, thin film nitinol and/or biodegradable polymer. A structural frame is formed of individual elongated pieces composed of biodegradable metal. These pieces are joined together by connector pieces composed of superelastic material. At least a portion of the structural frame has deposited thereon the thin film nitinol and/or biodegradable polymer. The structural frame of the device is collapsible for insertion in a delivery tube and, recoverable for deployment and placement in a vascular location of a patient body.

Implantable devices may include a single, first component or a plurality of components such as first and second components, the second component being flexibly coupled to the first component. A socket extends over one or more of the component(s), the socket being configured to enhance the inter-component interaction and/or including one or more exposed surface(s) configured to exhibit one or more tiers of foreign body responses within a range of possible foreign body responses.

A method for implanting a non-invasively and post-operatively adjustable penile implant in a penis of a patient, the implant comprising an expandable portion having a hollow portion adapted to receive a fluid, thereby allowing the expandable portion to be adjustable from a collapsed state into an expanded state. The method comprises the steps of: placing a proximal portion of said hollow portion in at least one corpus cavernosum, such that said proximal portion substantially extend on the inside of the male person when implanted in the penis; placing a distal portion of said hollow portion in the at least one corpus cavernosum such that said distal portion substantially extends on the outside of the male person when implanted in the penis, wherein the distal portion is placed with an invagination extending into the hollow portion in the collapsed state, and wherein said invagination is adapted to expand the hollow body in a length direction of the penile implant in the expanded state.

According to an aspect, an inflatable penile prosthesis includes a fluid reservoir configured to hold fluid, an inflatable member, and a pump assembly configured to transfer the fluid between the fluid reservoir and the inflatable member. The pump assembly includes a valve body having one or more valves, and an outer protective casing disposed over the valve body.

An implant material having an implant surface comprising a plurality of tissue-contacting members arranged in a regular or irregular two-dimensional array, each tissue-contacting member having a convex curved tissue-contacting surface. Methods of preparing and using such implant materials.

A stent for aorta is formed by weaving at least two types of filaments having different diameters, such as a first filament and a second filament. The stent is configured to be at least partially compressible and extensible along the axial direction of the stent in a natural release state, wherein the first filament has a diameter of 20-150 μm, and the second filament has a diameter of 150-800 μm. When the stent is used in the treatment of aortic aneurysm and/or aortic dissection lesions, due to the axial compressibility and extensibility of the stent, low liquid permeability and strong radial support force are provided where needed in the aorta, and due to the axial stretchability thereof, the stent can be easily assembled to a delivery system having an appropriate diameter. Also provided are a stent kit comprising the stent and a stent delivery system.