Abstract: A filter comprises an inner, anchoring basket arranged concentrically inside an outer, alignment basket. The anchoring basket comprises a plurality of anchoring struts terminating in barbs. The alignment basket includes a plurality of alignment struts, which terminate downstream of the anchoring struts. A lumen is provided through hubs of the filter so that the filter can be deployed over a guidewire.

Abstract: Apparatus and methods are described, including apparatus for puncturing a fossa ovalis of a heart. The apparatus includes a catheter shaped to define a catheter lumen. A puncturing element is slidably disposed within the catheter lumen, and is deployed from a distal portion of the catheter and to puncture the fossa ovalis. A probing element is deployed from the distal portion of the catheter. Upon being deployed, the probing element probes tissue near the fossa ovalis, the probing element having a first configuration thereof upon probing the tissue near the fossa ovalis. Upon probing tissue of the fossa ovalis, the probing element facilitates positioning of the puncturing element, by automatically adopting a second configuration thereof that is different from the first configuration. Other applications are also described.

Abstract: A sinus passage expansion device includes a pair of protruding tubular members connected to a base member. Each tubular member is split into hollow half portions each providing outwardly bulging forms which emulate an inner profile of a nasal cavity. The members are preferably made using a material having shape changing temperature sensitive properties. The base provides screen-covered apertures.

Abstract: A surgical instrument includes a handle assembly, an elongate body, a tool assembly, and an electrical energy source. The handle assembly includes an actuation knob. The elongate body extends distally from the handle assembly and defines a longitudinal axis. In particular, tool assembly is operatively coupled to the handle assembly and extends from a distal end of the elongate body. The tool assembly includes first and second jaw members each including an electrically conductive cutting element. The cutting elements are operatively coupled to the actuation knob. In particular, the cutting elements are movable between a first position in which the cutting elements are disposed within the respective jaw members and a second position in which the cutting elements extend out of the respective jaw members and are in general vertical registration with each other such that electrical energy can be transferred from the first jaw member to the second jaw member.

Abstract: The described invention provides an endovascular stent device comprising a tubular structure comprising a circumference; wherein a flow-diverting portion of the circumference is covered by a flow-diverting material; a length (l) from a proximal end to a distal end; and an inner diameter (d); wherein the flow-diverting portion of the circumference comprises a length (l?); and the flow-diverting portion of the circumference covers at least 1% to at least 100% of the endovascular stent device. According to some embodiments, the flow-diverting material is adapted to increase blood vessel wall adherence and minimize risk of an endoleak.

Abstract: A baby feeding pacifier includes a mounting base in the form of a mouth shield and a pedestal formed on the mouth shield, an annular seat affixed on the pedestal, a support member in the form of an elongated pole also affixed on the pedestal and extending beyond the annular seat, a hollow nipple that has pores between interior and exterior surfaces thereof and inserts into an installed position on the pedestal about the annular seat and the support pole, and a body configured to provide a material adapted for human consumption within and accessible through the pores of the hollow nipple and that seats on the annular seat and fits about the elongated support pole.

Abstract: A system, delivery device and method delivers ultrasonic energy to a target musculoskeletal tissue site. In some embodiments, the delivery device includes a stainless steel needle joined to a horn. In some embodiments, the stainless steel needle is joined to the horn using a heating process or a brazing process.

Abstract: A vascular closure device (20) having a proximal end and a distal end is described. The vascular closure device may include an insertion sheath (28), a handle, and a locator anchor (38) positionable distally outside a distal end of the insertion sheath when the handle is in a first position. The handle may be movable from the first position to a second position located proximally relative to the first position, the locator anchor being configured to expand laterally when the handle is moved from the first position to the second position. Additionally, the handle may be movable from the second position to a third position located proximally relative to the second position to deploy a vascular closure implant in a puncture tract. A vascular closure method is also disclosed.

Abstract: A lancet removal mechanism for a blood sampling device contains: a stop assembly, a trigger unit, and a control button. The stop assembly includes an inner protrusion. The trigger unit includes a lancet holder and a triggering shaft, wherein the lancet holder is fixed in the stop assembly and has an outer protrusion formed on an outer wall thereof to engage with the inner protrusion of the stop assembly, the lancet holder has an orifice defined therein, and the orifice has a first inner shoulder arranged on a top end thereof, the triggering shaft extends into the orifice of the lancet holder and has a first outer shoulder for engaging with the first inner shoulder of the lancet holder. Furthermore, the control button is fitted on a top end of the triggering shaft.

Abstract: This disclosure relates to elongated needle assemblies and methods of their manufacture and use.

Abstract: Systems, devices, and methods are provided for securing soft tissue to bone. One exemplary embodiment of a device includes an anchor, a repair filament, and a connecting filament that is coupled to the repair filament, is in contact with the anchor's distal end, and is effective to connect the repair filament to the anchor such that the repair filament slides with respect to the anchor. The anchor can be rigid, and can include an axial bore extending therethrough. At least one of the repair filament and the connecting filament can extend through at least a portion of the axial bore, and the bore can be sized such that a portion of the filament extending therethrough barely fits to help maintain the connection between the anchor, repair filament, and connecting filament. Embodiments of the systems and devices disclosed can be used in a number of methods for repairing soft tissue.

Abstract: The invention relates to a compression unit adapted to be arranged around a patient's forearm to provide pressure to a radial artery puncture site, wherein the compression unit comprises a unit attachment band provided with a frame, and a compression element in the shape of an inflatable bladder, the compression element is further adapted to be arranged within said frame, such that when the compression unit is arranged around a patient's forearm, the compression element provides pressure to the puncture wound when the compression element is inflated. The invention also relates to a radial artery compression system.

Abstract: A device for closure of an opening in a medical patient's blood vessel wall is disclosed. It discloses a plug shaft which is: porous; blood absorbing; insertable in an opening in a blood vessel wall; and, at least partially comprises an ECM material. A first cap which is integral with the plug shaft at a proximal end thereof is disclosed. A second cap is integral with the plug shaft. An insertion tube, a pusher, surgical methods of use, and kits, are also disclosed.

Abstract: A biomedical shape-set textile structure based mechanical thrombectomy systems and methods are described. In one of the embodiments, the mechanical thrombectomy device can be customized to the length of the clot in each patient. In one of the embodiments, the mechanical thrombectomy device because of the textile structure has a very low overall profile or thickness that is less than 0.0125 inches (0.317 mm) and therefore can be deployed within microcatheters with inner lumen diameter as small as 0.014 inches (0.355 mm).

Abstract: Tourniquet devices and associated methods of use and manufacture are disclosed herein. Tourniquet devices configured in accordance with several embodiments of the disclosure can include, for example, a strap having a proximal end portion and a distal end portion, a buckle assembly connected to the proximal end portion, and a pulley assembly movably coupled to the strap. Tourniquet devices configured in accordance with the technology can be easily applied because the pulley assemblies can reduce the force a user must exert on the tourniquet devices to constrict or occlude blood flow. Additionally, tourniquet devices disclosed herein can also serve as functional, wearable items (e.g., a belt, integrated into clothing) such that the tourniquet devices are conveniently stored and readily accessible in emergencies.

Abstract: A suturing device is disclosed. The suturing device includes an end effector assembly disposed on a distal end of the suturing device. The end effector assembly includes at least one guide tube housing at least one elongated member, a clamshell, and a probe configured for disposal in a graft tubular tissue circumferentially offset from the clamshell. The probe includes at least one guide tube attached to a suture having a first end and a second end. The at least one elongated member is deployed to puncture graft tubular tissue and mate with the at least one aperture of the probe such that extraction of the at least one elongated member simultaneously draws out the suture through the punctured graft tubular tissue.

Abstract: The disclosure pertains to debris diverters for use within the aorta and methods of diverting or redirecting emboli and other debris away from the carotid arteries to prevent cerebral embolization. The disclosure includes aortic diverters positionable in the ascending aorta in order to divert embolic material of all sizes away from the carotid arteries, thereby washing emboli downstream into the thoracic and peripheral vasculature. The debris diverters of the disclosure are adapted to be placed in the ascending and transverse aorta via the left subclavian artery in order to divert embolic material away from the carotid arteries and methods of use therefor.

Abstract: The present disclosure provides a deployment device that includes (a) an elongate shaft having a first end and a second end, (b) a grasping assembly coupled to the first end of the elongate shaft, where the grasping assembly includes a first jaw and a second jaw rotatable with respect to the elongate shaft, where the grasping assembly is configured to accept a wound closure device between the first jaw and the second jaw, where the wound closure device comprises at least two fixation components connected to and extending therethrough, where each of the first jaw and the second jaw include at least one coupling element configured to be removably coupled to a respective fixation component when the wound closure device is coupled to the grasping assembly, and (c) an actuator coupled to the second end of the elongate shaft, where the actuator is configured to move the grasping assembly between an open position and a closed position.

Abstract: Improved catheter devices for delivery, repositioning and/or percutaneous retrieval of percutaneously implanted heart valves are described, including a medical device handle that provides an array of features helpful in conducting a percutaneous heart valve implantation procedure while variously enabling radial expansion or contraction and/or lateral positioning control over the heart valve during the medical procedure.

Abstract: A device (100) for arrangement on the side wall of an intestine is provided. The device (100) comprises a first member (10) and a second member (20) of a generally hollow open configuration. The first member (10) comprises an elastic part (11), with a first and a second axial end, and a rigid support part (12), arranged at the first axial end of the elastic part (11). The second member (20) comprises a first and a second axial end, said first end of the second member (20) matching the shape of the second axial end of the elastic part (11), such that an intestine wall may be uniformly distributed between the second axial end of the elastic part (11) and the second member (20). The device (100) also comprises a connection member (30) for connecting the rigid support part (12) and the second member (20) to each other. A method for arranging said device at the side wall of a tubular structure, and a connector (200) for connecting two devices (100) is also provided.