Abstract: A vessel filter comprising a first region and a second region wherein the filter is movable between a collapsed position for delivery to the vessel and an expanded position for placement within the vessel. A first region has a filter portion having a converging region at a first end portion to direct particles toward the center of the filter and the second region is flared in the expanded position to have a transverse dimension increasing toward a second end portion opposite the first end portion. The second region includes a vessel engaging portion at the second end portion. The second region includes a plurality of spaced apart struts with adjacent struts being joined.

Abstract: A medical device having at least one static state, at least activated state, and at least one active region including electroactive polymer (EAP) capable of fine electro-activated movements. The EAP movements include bending components for proper alignment, rotating components for pooper fittings, making components more rigid or flexible, and increasing and decreasing the volume of components. The fine movements allow for highly versatile and adaptable medical devices.

Abstract: A vascular graft comprises a perforate tubular compressible frame having a fabric liner disposed over at least a portion of the frames lumen. The graft may be used in combination with a base structure to form a bifurcated graft in situ. The base structure compresses a compressible frame having a fabric liner which defines a pair of divergent legs. The base structure is positioned within the aorta so that one leg enters each iliac. The tubular grafts can then be introduced into each leg to form the bifurcated structure. A graft delivery catheter includes a controllably flared sheath which facilitates recapture of a partially deployed graft.

Abstract: The present invention relates to compositions and structure of deformable alloys on the basis of magnesium with an optimum combination of mechanical properties (strength, plasticity) and a resistance to corrosion, including in vivo. Alloys of the new group possess an excellent formability at room temperature, high corrosion stability in sodium chloride solution, excellent heat resistance and can be used in various technical applications, particularly in vivo as a structural material for stents.

Abstract: The invention is a method of delivering and deploying a tissue shaping device in a lumen within a patient, with the tissue shaping device including an anchor. In some embodiments the method includes the steps of: inserting a delivery catheter into the lumen; percutaneously delivering the device to a target site within the lumen through a delivery catheter; operating an actuator to expose an anchor; and operating the actuator to lock the anchor. In other, the method includes the steps of: inserting a delivery catheter into the lumen; moving the device from a cartridge into the delivery catheter; delivering the device to a target site within the lumen; operating an actuator to move the delivery catheter with respect to the anchor to expose the anchor; and expanding the anchor.

Abstract: A localizing wire includes an anchor portion that can change shape from a collapsed shape to an expanded shape and thereby anchor within a tissue mass. The localizing wire has an exterior portion that can lie flat against the tissue mass. The localizing wire can be repositioned or withdrawn without the need for the reinsertion of an introducer.

Abstract: A vessel filter having a first region and a second region, the filter movable between a collapsed position for delivery to the vessel and an expanded position for placement within the vessel. The first region has a filter portion having a converging region to direct particles toward the center of the filter and includes a plurality of spaced apart filter struts. The struts each have a strut height defined as a distance between a first wall and a second wall. A plurality of hooks are at the second region, the hooks having a vessel penetrating tip and a width greater than the width of the strut from which it extends such that the penetrating tip portion of the hook extends beyond the first wall.

Abstract: A forceps that includes a housing, a cutting assembly, and an actuator. The housing has a shaft attached thereto that extends therefrom and is configured to support a pair of jaw members at a distal end thereof. The jaw members are movable to grasp tissue therebetween. The cutting assembly includes a spring element that has proximal and distal ends. The proximal end of the spring element is fixed to a boss disposed within the housing and the distal end of the spring element includes a cutting edge. The spring element is coiled at a proximal end thereof to create a spring bias against the boss. The actuator is operably coupled to the spring element and is configured to selectively advance the cutting edge of the spring element into the jaw members against the spring bias to sever tissue disposed therebetween.

Abstract: A spatula for depilatory use comprises a generally S-section flexible plastics body 4, a straight elastomeric fin 10 at one end, and at the other end, an elastomeric fin of “fish-tail” shape. The straight fin can remove a depilatory preparation from most areas of the skin, and the other fin is able to remove the preparation from less accessible areas. The elastomeric fins give effective hair removal while avoiding the deleterious effects of earlier scrapers.

Abstract: A surgical obturator is disclosed comprising an elongate shaft extending along an axis between a proximal end and a distal end, and a bladeless tip disposed at the distal end of the shaft. The bladeless tip has a conical surface forming proximally into an outer surface, the outer surface extending distally to a blunt point and having a pair of side sections. The side sections extend from the blunt point radially outwardly with progressive positions proximally along the axis. The conical surface facilitates insertion of the obturator with a reduced penetration force and minimizes tenting of the body wall. The conical surface further facilitates separation of different layers of the body wall and provides proper alignment of the tip between the layers.

Abstract: A lancet is pressed against a puncture needle cartridge while fitting a puncture needle loading inlet of the lancet to the axis of a puncture needle on the puncture needle cartridge. In order to facilitate the operation, one of plural puncture needles, arranged in parallel, is tilted up from its initial position at a predetermined angle, and the puncture needle is guided into a puncture needle holding rod of the lancet. Simultaneously, the puncture needle is pressed up to a position where the rear end part of the needle pushes the bottom surface of a puncture needle loading chamber of the puncture needle holding rod, whereby the puncture needle is loaded. When discarding a used puncture needle, the puncture needle is inserted into a lancet guide member of the puncture needle cartridge, whereby the puncture needle is reliably captured to be discarded.

Abstract: A surgical instrument featuring a combination cauterizing and surgical capture component. The instrument is deployable from a distal end of a lumen to a first position partially exposing a cauterizing loop and restrained radially deployable members wherein a plurality of cauterizations may be performed. The instrument is deployable to a second position fully translated from the lumen wherein the plurality of radially positionable members may be released by activation of a release member to allow the biased members to deploy radially around an axis running through the loop.

Abstract: A removable stent for placement within a lumen is provided. The stent includes a scaffolding of struts configured to define a substantially cylindrical member having a proximal end and a distal end. The stent also includes at least one flexible element spirally wound along at least a portion of a respective strut, wherein the element comprises at least one engageable member such that a force applied to the engageable member does not result in purse-stringing.

Abstract: A surgical portal apparatus includes a portal housing, an elongated portal member connected to the portal housing and an armature assembly. The portal housing and the portal member have an axial bore for reception and passage of a surgical object. The armature assembly includes at least two arms disposed within the portal housing and an outer mount. The at least two arms extend at least radially inwardly and are adapted to move relative to the longitudinal axis from a rest position to an activated position during passage of the surgical object. The at least two arms are operatively connected whereby movement of a first arm causes corresponding movement of a second arm. The outer mount comprises a resilient material and is mounted to the at least two arms, and imparts a biasing force thereto toward the rest position.

Abstract: Tools and methods are provided for removing biological units from a body surface utilizing a removal tool. The tools may incorporate retention members and mechanisms configured to impede movement of the biological unit in the direction of a distal end of the tool and to improve retention of the biological unit in the tool. Some of the retention members are stationary and some are movable within the lumen of the biological unit removal tools. The distal tips of the tools are desirably configured to reduce the chance of transection of a biological unit, such as by including both cutting segments and blunt relief segments. A number of dual concentric tube embodiments permit a division of removal functions. Distal fluid or gas delivery may supplement a vacuum in a luminal space to help extract biological units from surrounding tissue.

Abstract: A system for occluding a physical anomaly. One embodiment comprises a shape memory material body wherein the shape memory material body fits within the physical anomaly occluding the physical anomaly. The shape memory material body has a primary shape for occluding the physical anomaly and a secondary shape for being positioned in the physical anomaly.

Abstract: A medical instrument has a shaft. The shaft has an outer shaft and an inner shaft. The outer shaft encloses the inner shaft. The medical instrument further has an actuator for rotating the inner shaft about a longitudinal axis relative to the outer shaft, arranged at a proximal end region of the shaft. The medical instrument has at least two tappet elements for transferring a rotary movement of the actuator to the inner shaft, which are engaged interchangeably with the inner shaft for transferring the rotary movement of the actuator to the inner shaft. The tappet elements reach through peripherally limited openings in a proximal end region of the outer shaft, which openings are offset with respect to one another in the longitudinal direction.

Abstract: A cutter (8) is telescopically received in a cannula (9) and both the cutter and cannula are telescopically mounted on a tubular carrier (7). A detection device (6) may be inserted through the open-ended carrier, cutter and cannula to properly place the surgical instrument in alignment with the tumor to be excised. Positioning tines (80) may penetrate the patient to firmly locate the carrier in its proper position on the patient. The cutter and cannula are moved about the carrier and are pressed into the tissue of the patient with the expectation that the circular core (60) of breast tissue formed by the cutter will have clear margins about the tumor. If the tumor extends too close to the circular incision, the cannula may be rotated so that its sidewall opening (26) faces the side of the remaining tissue to be excised and the surgeon can pull the remaining tissue through the sidewall and excise it, thereby avoiding a separate and delayed surgical procedure.

Abstract: A modular, reduced-pressure, wound-closure system for generating a closing force on a surface wound on a patient includes a sealed contracting member, a plurality of attachment base members, and a plurality of connecting members. The combination of the plurality of attachment base members and plurality of connecting members forms a circumferential wall around the surface wound. The sealed contracting member is operable to be disposed within an interior space defined by the circumferential wall and coupled to at least of portion of the circumferential wall. When reduced pressure is provided to the sealed contracting member, the sealed contracting member contracts and the circumferential wall delivers a closing force. Other systems and methods are presented.

Abstract: Described is a device useful for applying compression to the eyes and regions under the eyes of a user. In one form, such a compression device includes a relatively elongate compression body combined with a strap for receipt around the head of a user. The relatively elongate compression body includes a central region for receipt over the face of a user, as well as flanking regions for receipt over the side of the face and the ears of the user, substantially encircling the head. Preferred devices include compression bodies having pockets containing compression inserts and positioned to contact the eyes and under-eye tissues of the user, desirably having openings in a location other than at an edge of the pockets, e.g. provided by a central slit. Compression inserts may include foam pads or conformable membrane shells encasing a flowable fluid or other substance.