Abstract: This invention relates to a blood lancet device that is used to collect a small quantity of blood from a human body. More specifically, it relates to a blood lancet device that: can control the depth of the lancet needle's penetration of the skin; can push the lancet to eject; can accurately collect blood by ensuring linear motion; and can reduce the pain involved in blood collection.

Abstract: A stent graft (1) with an internal tube (15) extending from the fenestration (11) within and towards an end of the tubular body (3) of the stent graft. An end of the tube remote from the fenestration is flared into a funnel or elliptical shape (17) to facilitate access into the internal tube from a main lumen of the stent graft. The flared portion is fastened (19) to the wall of the stent graft. The flared portion is held open with a resilient wire ring (21).

Abstract: A composite end effector for an ultrasonic surgical instrument is provided and includes a first portion formed from a first material that exhibits a first characteristic value when excited by an ultrasonic energy input and a second portion formed from a second material that exhibits a second characteristic value when excited by the ultrasonic energy input. The composite end effector exhibits a composite characteristic value different from the first and second characteristic values when excited by the ultrasonic energy input.

Abstract: Tweezers for cosmetic use having two branches (3) with one metallic extremity (2) for seizing small objects, the maximum width of both branches (3) being greater than half the average width of the resting surface of the thumb of an adult user of average corpulence when said tweezers are actuated, and the maximum length of both branches (3) being less than the average length of the thumb of an adult of average corpulence. Even a person of reduced dexterity is thus capable of easily holding the inventive tweezers between two fingers to close them. Furthermore, the width of the branches (3) prevents the latter from sliding between the user's fingers and/or the tweezers from turning involuntarily when they are closed, even strongly or askew.

Abstract: The present invention provides a medical balloon having enlarged radii, which may be disposed on a dilation catheter. The enlarged radii balloon may reduce the trauma experienced by a patient both during the procedure and when the catheter is removed from the patient. The enlarged radii may provide the deflated balloon with smoother transitions and less mechanical rigidity at the balloon transitions.

Abstract: A method of removing an implanted vessel filter by a femoral approach comprising the steps of providing a catheter, inserting a curved device into the catheter to a position proximal of the tip, advancing the catheter tip through the femoral vein and past a cranial end of the filter, inserting the curved device into the catheter tip to move the catheter tip to a more curved position, and inserting a filter grasping device though the curved device and catheter tip to exit a distal portion to grasp the filter.

Abstract: An active annuloplasty ring holder having a template that can be folded or pivoted to the side allowing the template to align longitudinally with the handle and enter the patient's chest through a small incision. The holder may include a mechanism to remotely detach sutures fastening the ring to the holder, thereby detaching the ring while avoiding the risk associated with introducing a scalpel into the operating field. A detachment mechanism may include a movable pin actuated by a pull wire that releases a plurality of holding sutures, or a hot wire, knives, or pull wire that severs the sutures. The holder may have a built-in light source for better visualization of the ring inside the heart. The holder may also have an optical means of visualizing the inside of the heart from the proximal end of the handle.

Abstract: Percutaneous methods and apparatus for forming a venous valve from autologous tissue by creating at least one subintimal longitudinal dissection that forms at least one flap of intimal tissue are disclosed. In one method, a balloon catheter having a dissecting blade mounted thereon is delivered to a target site where a new venous valve is to be created. The balloon is inflated to deploy the blade against the vein wall, and the catheter is longitudinally translated such that the blade dissects a subintimal layer of the vein wall. The balloon is subsequently deflated such that the blade pulls a flap of the dissected tissue towards the vein lumen, thereby creating a leaflet and corresponding pocket/sinus in the vein that collectively act as a monocuspid venous valve. Methods of forming new bicuspid and tricuspid venous valves utilizing two or three dissecting blades mounted on the balloon are also disclosed.

Abstract: A surgical system includes a surgical instrument including a conducting section transmitting ultrasound vibration generated by an ultrasound transducer to a distal end portion and transmitting a high-frequency output signal to the distal end portion, an ultrasound drive section outputting an ultrasound drive signal to the ultrasound transducer, a high-frequency output section outputting a high-frequency output signal to the conducting section, a detection section detecting an ultrasound impedance of a surgical site to which ultrasound energy and high-frequency energy are provided from the distal end portion by outputting both signals simultaneously to the surgical instrument, a determination section determining whether the detected ultrasound impedance is in a predetermined range, and a control section performing control to increase a high-frequency output value by a first predetermined amount or decrease the high-frequency output value by a second predetermined amount when the detected ultrasound impedance i

Abstract: An apparatus for tissue repair includes first and second fixation members configured to secure tissue together, a flexible coupling member coupling the first and second fixation members, the flexible coupling member having two terminal ends, one of the two terminal ends terminating adjacent one of the first and second fixation members, the flexible coupling member slidably coupled to at least one of the first and second fixation members such that when the other of the two terminal ends of the flexible coupling member is pulled, a length of the flexible coupling member between the first and second fixation members is shortened, and a closed loop of flexible material, the flexible coupling member being slidably received through the closed loop of flexible material.

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 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 first region includes a plurality of spaced apart elongated struts with adjacent struts being joined.

Abstract: A vascular occlusion device that includes a central support member that has at least one mesh embolic ribbon extending outwardly from the central support member in the generally radial direction is provided. The mesh embolic ribbon has a collapsed and an expanded configuration.

Abstract: The radially deformable tubular prosthesis comprises a lattice that is deformable between a retracted state of small diameter and an expanded state of greater diameter. It includes at least two external hooks defining between them a clamp for hooking in external tissue, the two hooks being carried by the lattice and being movable between a spaced-apart position in which the clamp is open, and a closer-together position in which the clamp is closed.

Abstract: A surgical blade is disclosed for use with a surgical tool for making incisions in the sclera of an eye to form a scleral pocket to receive a scleral prosthesis. The surgical blade comprises a rotatable support arm capable of being rotated by the surgical tool and a detachable curved cutting blade for making incisions in the sclera of an eye. The surgical tool causes the curved cutting blade to advance through the sclera to form an incision having dimensions to receive a scleral prosthesis. When the incision is complete the curved cutting blade is detached from the rotatable support arm. The curved cutting blade is then removed from the incision by pulling the curved cutting blade forward out of the incision. The incision has the exact dimensions to receive a scleral prosthesis.

Abstract: A method for suturing a patent foramen ovale (PFO) includes providing a suturing device, advancing the suturing device through the inferior vena cava, right atrium, and PFO such that a first foot of the device is positioned in the left atrium, deploying the first foot to a deployed position, orienting the suturing device such that a distal portion of tissue of the PFO is received in a pre-formed curve portion of a foot housing of the device, advancing the first needle through tissue and further into a first needle receptacle disposed on the first foot, and advancing at least one end of the length of suture through the tissue to suture the PFO.

Abstract: A stent graft device for implanting in a body lumen, comprising a stent with non-staggered or staggered apexes, said stent comprising a plurality of stent sections, bendable connecting members forming said non-staggered or staggered apexes and connecting each of said stent sections to other stent sections to form a zigzag pattern, wherein said stent is staggerdly sutured to a graft by a plurality of suture knots, and wherein said suture knots and staggered apexes are staggered when said stent sections are crimped, and methods of use thereof.

Abstract: A clot retrieval device including a self-expandable member having a proximal end portion and a main body portion. The self-expandable member is expandable from a first delivery position to a second placement position. In the first delivery position the expandable member has a first overall diameter In one implementation the cell structures that form the self-expandable member have dimensional and material characteristics that result in about a ?1.0N to about a ?1.7N overall reduction in radial force along the length of the expandable member per millimeter of expansion during about an initial 0.50 mm diametric range of expansion from the first overall diameter and that results in about a ?0.10N to about a ?0.35N overall reduction in radial force along the length of the expandable member per millimeter of expansion during subsequent diametric ranges of expansion.

Abstract: Provided is a wound closure assisting and maintaining apparatus that can be attached to a wide open wound of a patient and can stretch skin around the wound gradually to achieve the wound closure and maintain the wound closure during most critical postoperative period. The apparatus includes: a loop suture being threaded through skin; a tightening member for gathering both ends of the threaded loop suture at one point and for exerting a pressure of wound tightening force evenly on skin; a pulling member for pulling the loop suture in order to tighten the threaded loop suture; a housing member for housing the pulling member and making the loop suture tightened by transformation of a pulling force to a wound tightening force when pulling member pulls the loop suture out of skin; and a locking member for fixing a position of the pulling member to maintain the tightened status.

Abstract: A device for deploying a cardiac valve prosthesis includes a distal valve holder portion and a shaft extending towards the valve holder portion. The shaft is selectively bendable to a curved shape to vary the spatial orientation of the valve holder portion with respect to the desired implantation site.

Abstract: A single use lancet device having a housing, with an open interior and an access opening defined therein, a lancet, with a body and a piercing tip, and disposed in the open interior of the housing so as to move between a cocked orientation and a piercing orientation, a driving assembly structured to move the lancet into the piercing orientation, and a restrictor assembly having a shoulder element and a restrictor panel operatively associated with the lancet and the housing and structured to pass over the restrictor panel upon the lancet moving from its cocked orientation to its piercing orientation, and to abut the restrictor panel upon attempted movement of the lancet back into its cocked orientation after movement into the piercing orientation, thereby preventing the lancet from moving back into the cocked orientation and preventing re-use of a contaminated piercing tip.