A breast implant system comprises at least one casing (3, 4) with a flexible outer shape for implantation in a patient's body so as to form part of a breast implant (10) and further comprises at least one first element (1) contained in the casing and optionally at least one second element (2) also contained in the casing. The first and second elements are either displaceable within the casing and/or their volume can be changed in order to change the shape and/or size of the breast implant. A reservoir (R) comprising a lubricating fluid is connected to the casing so as to allow lubricating fluid to be supplied to and removed from the casing in order to reduce surface friction between adjacent elements and/or between the casing and the elements before the shape of the breast implant is changed.

A delivery system and a method for deploying a cardiovascular prosthetic implant using a minimally invasive procedure are disclosed. The delivery system comprises an introducer catheter, a delivery catheter having a proximal end and a distal end, and a seal assembly, wherein an outer diameter of the distal end of the delivery catheter is greater than an inner diameter of the distal end of the introducer catheter.

Systems and methods for treating diseased bodily lumens involving branched lumen deployment sites include a main graft or stent-graft deployable in a main artery and a vent device or stent-graft deployable in a branch artery to maintain blood flow through the main artery and from the main artery to the branch artery. Systems and methods for treating diseased bodily lumens involving branched lumen deployment sites may also include a main graft or stent-graft deployable in the main artery, a chimney graft or stent-graft deployable in both branch artery and the main artery to the branch artery and a gutter-sealing device associated with the chimney graft to prevent flow of blood among the chimney graft, the main graft and a wall of the main artery.

The present disclosure relates to a system and method of knee ligament balancing for knee replacement procedures. The disclosure provides a system of components to implant to achieve ligament balancing. In addition, instruments and methods are provided to achieve the desired balance of the ligaments before final fixation.

An artificial urinary sphincter (AUS) system that includes an elastic tube to be wrapped around a urethra and having at least one connector. The elastic tube has a first end to receive and dispatch fluid and a second end to be connected to the at least one connector. The elastic tube receives and dispatches the fluid to expand and contract the elastic tube and to coapt the urethra for continence and open the urethra for voiding.

An orthotopic artificial bladder endoprosthesis includes a casing made of a PGA fiber fabric; the casing having two first connectors for the connection with the ureters of a patient and a further connector for the connection with the urethra of a patient; an inflatable element inserted in the casing; the inflatable element being switchable between an inflated configuration, in which it supports and maintains in position the casing, and a deflated configuration.

Systems, devices and methods for repairing a native heart valve. In one embodiment, a repair device for repairing a native mitral valve having an anterior leaflet and a posterior leaflet between a left atrium and a left ventricle comprises a support having a contracted configuration and an extended configuration. In the contracted configuration, the support is sized to be inserted under the posterior leaflet between a wall of the left ventricle and chordae tendineae. In the extended configuration, the support is configured to project anteriorly with respect to a posterior wall of the left ventricle by a distance sufficient to position at least a portion of the posterior leaflet toward the anterior leaflet.

Linings for fitting an object to a body part, and their use, are provided. The lining may include a flexible sheet having a fluid impenetrable outer portion enclosing an internal volume and the lining may include barriers forming a number of compartments substantially secured in place within the internal volume. The barriers may be permeable to gas and/or liquid, yet may be impermeable to the conformable material and the gas and/or liquid may be supplied to or aspirated from one or more compartments within the internal volume. Aspiration of gas and/or liquid from the internal volume may limit both deformation of the conformable material and shape adjustment of the flexible sheet.

Apparatus, including an enclosure, a fluid-tight bag located within the enclosure, and a fluid-tight valve connected to the fluid-tight bag. The apparatus also has a tube, having a first end connected to the fluid-tight bag via the fluid-tight valve, and a second end connected to a balloon within a breast implant fitted to an implantee. The apparatus further includes a spindle, located within the enclosure, connected to the fluid-tight bag, and configured to rotate under control of the implantee so as to roll the fluid-tight bag onto the spindle or to unroll the fluid-tight bag from the spindle, and thus transfer a fluid, contained in the balloon, the tube, and the fluid-tight bag, therebetween.

The invention relates to a method for the manufacture of a breast prosthesis, comprising: providing and superimposing inner and outer plastic foils; welding together the plastic foils to form the circumferential welding seam, thereby leaving a gap to form a filling channel connecting the inner space to an outside; filling the inner space with a fluid curable mass, which is a precursor of the filler material, by injecting the fluid curable mass into the inner space through the filling channel; and curing the fluid curable mass inside the inner space to form the filler material; wherein the filling channel is provided with a check valve to prevent fluid curable mass from entering the filling channel after injection. The invention additionally proposes a breast prosthesis made by such method.