Abstract: A retrievable device for treatment of a stenotic lesion in a body vessel is disclosed. The device comprises a reticulation portion including a plurality of struts connected together in a singly staggered configuration distally along a longitudinal axis. The plurality of struts of the reticulation portion is configured to fold along the longitudinal axis defining a collapsed state of the device for retrieval. The device further includes an expandable body distally extending from the reticulation portion along an outer diameter for treatment of the stenotic lesion. The expandable body is configured to expand in the open state and collapsed in the collapsed state of the reticulation portion for retrieval. The device further comprises a retrieval stem extending proximally from the reticulation portion for retrieval of the device in the collapsed state.

Abstract: A portable lancing aid for providing liquid samples comprises a lancet system having at least one lancet, a tensioning device, and an electromechanical actuator. The tensioning device can be tensioned by the electromechanical actuator. The portable lancing aid may further include an energy source for storing electrical energy that is connected to the electromechanical actuator. Additionally, the portable lancing aid may include an interface for charging the energy source where the interface is externally accessible from the lancet system. The invention is ergonomical and easy to handle for children and patients with physical limitations. Furthermore, a lancing system for collecting liquid samples is provided with a portable lancing aid that is detachably mountable to a charging station for charging the portable lancing aid.

Abstract: A trocar is described. The trocar is formed of a biocompatible material, such as but not limited to stainless steel. Accordingly, the trocar is reusable for a relatively large number of surgical procedures assuming conventional sterilization techniques are employed after each surgical procedure. Additionally, the trocar is provided with an angled blade design formed on a distal portion of the trocar shaft. More specifically, the blade design includes a first portion extending substantially co-planar to a proximal portion of the tip portion of the trocar shaft and a second portion extending angularly inwardly towards a distal portion of the tip portion of the trocar shaft.

Abstract: A stoma dilator having a base dilator and a plurality of dilators coaxially disposed over the base dilator. The base dilator has a hub and an opening therethrough. Each of the plurality of dilators has a tapered distal end, a proximal end, and a tubular body, and are held in separated, telescoping position by a dilator positioner such that part of each distal end is exposed from beneath another dilator and is graspable for movement such that a smaller dilator does not become inaccessible inside of a larger dilator. The stoma dilator includes a hollow sheath positioned over an outermost dilator to hold open a tissue opening created by the plurality of dilators. The base dilator and the plurality of dilators may be removed while the sheath remains in a tissue opening. Another device may be inserted through the sheath, and the sheath may be peeled away therefrom.

Abstract: An endoluminal prosthesis comprises a tubular body which can be expanded about a longitudinal axis. A plurality of serpentines extend in a substantially circumferential direction. Each comprises arm portions and bend portions which join two subsequent arms. The bends facing an adjacent serpentine are circumferentially offset relative to the respective opposite bends of the contiguous serpentine, both when the prosthesis is collapsed and when the prosthesis is expanded. A first portion comprises at least two adjacent serpentines interconnected by at least one bridge, and at least two bends situated at the shortest longitudinal distance between the two serpentines is not connected by a bridge. A second portion comprises at least two adjacent serpentines interconnected by a number of bridges equal to the number of pairs of bends of the two serpentines, at the shortest longitudinal distance between the two serpentines.

Abstract: Seal assemblies, generally for use in trocar assemblies, are provided for selectively promoting movement of fluid away from a central portion of the seal assemblies. In one exemplary embodiment, an inner surface of a seal body of the seal assembly is configured to selectively promote such movement of fluid away from the central portion of the seal body toward a peripheral portion of the seal body. While various configurations, geometries, and dimensions are discussed, one example of such a configuration includes locating a central portion of the seal body at a more proximal position than a peripheral portion of the seal body.

Abstract: A surgical instrument that absorbs fluid material on surfaces of a trocar is provided. The surgical instrument comprises a handle having at least two ends and an absorbent area at a first end of the handle. The absorbent area comprises a plurality of absorbent discs and a plurality of spacers.

Abstract: A surgical tool system. Various embodiments of the surgical tool system may comprise surgical instrument that has a handle assembly that operably supports a drive system therein for generating drive motions upon actuation of a movable handle portion operably coupled to the handle assembly. An elongated body protrudes from the handle assembly and operably supports a control rod therein that interfaces with the drive system. The surgical tool system further includes at least two surgical tools selected from the group of surgical tools consisting of: manipulators, nippers, scissors, endocutters, tissue thickness measurement devices, staple appliers, clip appliers, syringes for applying glue, sealant, drugs or medicaments and cauterization devices wherein each of the surgical tool within the group of surgical tools at least has a housing that is removably couplable to the elongated body and a drive assembly that is removably couplable to the control rod for receiving the drive motions therefrom.

Abstract: A clot removal device and method for removing a clot from a blood vessel may include an expandable clot engagement element, an expandable clot capture element, and a sheath surrounding and compressing the capture element and the engagement element. The sheath may be removable to thereby enable the capture element to expand in a blood vessel in which the sheath is deployed, and to enable the engagement element to expand within the capture element.

Abstract: An endoscopic needle device comprises a handle and a catheter sheath connected to the handle, wherein the catheter sheath has at least one lumen, for example a needle lumen and a stabilization lumen, extending therethrough. A needle is selectively movable within the needle lumen between a needle retracted position and a needle extended position and a stabilization element is selectively movable within the stabilization lumen between a stabilizer retracted position and a stabilizer extended position. A linking mechanism may operatively connect the needle and the stabilization element so that when the needle is in the needle retracted position the stabilization element is in the stabilizer extended position and when the needle is in the needle extended position the stabilization element is in the stabilizer retracted position.

Abstract: The invention relates to a monocanaliculonasal and/or monocanalicular intubation assembly particularly intended for lacrimonasal imperforation including a probe (1) made of a first material, in particular a flexible material such as silicone, the probe having a substantially cylindrical shape along a longitudinal axis; and a device for inserting the probe into a lacrimal canal or canaliculus. The device includes an insertion tube (10) made of a rigid material, such as a metal, having a distal end opening and a proximal end opening, the tube having a shape and a size enabling it to receive the probe therein; and a mandrel (20) for pushing the probe and expelling the same from the insertion tube by the distal end opening.

Abstract: Disclosed herein is a system for releasing a ligament. In one embodiment, the system includes a proximal handle, a tubular body, and a flexible body. The tubular body includes a proximal end and a distal end. The handle is coupled to the proximal end. The flexible body extends through the tubular body and includes a tissue cutting portion. The flexible body or tubular body is longitudinally displaceable to move the tissue cutting portion between a non-deployed state and a deployed state.

Abstract: Provided herein is an apparatus and method useful for surgical removal of mammalian tissue at specific depths and specific angles. In one or more implementations, an extraction instrument having a main body, a nipple portion, a punch, and an actuator may be utilized to extract one or more hair follicles.

Abstract: The invention relates to a system for ophthalmology or dermatology, having a laser unit for generating pulsed laser radiation, the pulse length of the laser pulses lying in the femtosecond range, a hand unit for emitting laser radiation generated by the laser unit, and a flexible light waveguide for delivering the laser radiation generated by the laser unit to the hand unit. The invention furthermore relates to a corresponding hand unit for emitting pulsed laser radiation generated by a laser unit, the laser radiation having pulse lengths in the femtosecond range.

Abstract: This invention is an endoluminal device including a stent; a tubular graft supported by the stent, wherein the graft comprises a proximal opening and a distal opening; and a variable diameter ring adjacent one of said openings, wherein the variable diameter ring comprises a coiled length of wire having two ends and forming at least one winding around the tubular graft. This invention also relates to the methods of treating an aneurysm and making the endoluminal device.

Abstract: Disclosed herein is a system for releasing a ligament. In one embodiment, the system includes a proximal handle, a tubular body, and a flexible body. The tubular body includes a proximal end and a distal end. The handle is coupled to the proximal end. The flexible body extends through the tubular body and includes a tissue cutting portion. The flexible body is longitudinally displaceable relative to the tubular body to move the tissue cutting portion between a non-deployed state and a deployed state.

Abstract: A deployment cartridge is provided to insert a coated stent into a junction formed between to tubular tissue sections. The deployment cartridge includes a pusher and a coated stent contained within the pusher. The pusher includes support structure for engagement with the stent. The stent is coated with a tissue sealant or tissue adhesive. An insertion instrument is also disclosed for advancing the deployment cartridge into the junction formed between the two tubular tissue sections. There is also disclosed a method of facilitating the support and healing at a juncture formed between tubular tissue sections with a coated stent.

Abstract: An improved stent-graft device is provided that delivers a smooth flow surface over a range of operative expanded diameters by applying a unique cover material to the stent through a technique that allows the cover to become wrinkle-free prior to reaching fully deployed diameter. The unique cover material then allows the device to continue to expand to a fully deployed diameter while maintaining a smooth and coherent flow surface throughout this additional expansion. Employed with a self-expanding device, when the device is unconstrained from a compacted diameter it will self-expand up to a fully deployed diameter with the graft being substantially wrinkle-free over diameters ranging from about 30-50% to 100% of the fully deployed diameter. Preferably, the graft component comprises an elastomeric material, such as silicone, polyurethane, or a copolymer of PAVE-TFE.

Abstract: A delivery catheter with a plug ejection mechanism with a fluid filled actuator incorporated in the catheter's handle is disclosed. After delivery of RF energy, the clinician deploys the plug within the region of the lesion by activating the plug ejection mechanism.

Abstract: A radially expandable system for the usage in body tubes is kept, by fixation of a first part and a second part relative to each other, in a second state in which the system exhibits a larger diameter compared to a first state. The fixation of the first part relative to the second part is performed by an adhesive. With the radially expandable system a body tube, for example a vein, can be assisted in its function. The first part and the second part can be arranged on or be formed by one single wall element or two different wall elements.