Abstract: Telescoping, self-driving, and laterally-pushing atherectomy devices are provided, each having a flexible sheath, a cutter with helical flutes, and a drive assembly. The drive assembly can have a flexible driveshaft rotatably translational with the lumen of the flexible sheath, a positive displacement pump to transport cut tissue, and a flexible drive shaft that can be longer than the flexible sheath for a reversible telescoping of the drive assembly from the lumen of the flexible sheath. The positive displacement pump can be a screw pump having a drive screw portion exposed for contact with a vascular lumen for a self-driving of the device through the vascular lumen. A reversibly-expandable, lateral pushing member can be included at the distal end of the flexible sheath for a lateral pushing of the cutter. Improved cutting heads, and methods of making them, are provided for cutting a combination of soft and hard plaque.

Abstract: Disclosed is a thrombectomy device with segmented design, and the device includes a thrombectomy net and a push rod fixedly connected with a proximal end of the thrombectomy net, where the thrombectomy net is a tubular hollow self-expanding net capable of automatically expanding radially, which is contracted after being compressed radially, and expands radially after a constraint of radial compression is released. The thrombectomy net includes a slope section, a thrombectomy section, and a gathering section which are sequentially connected from the proximal end to a distal end, where the thrombectomy section includes at least two thrombectomy subsections which are sequentially connected from the proximal end to the distal end and are relatively independent, and two adjacent thrombectomy subsections are locally connected, so that the two adjacent thrombectomy subsections are relatively independent during radial expansion.

Abstract: A medical device and a method of operating the same are provided. In a method of operating a medical device for ultrasonic treatment, the medical device including an ultrasonic instrument having a vibration transmission member that vibrates ultrasonically, a power source configured to supply electric energy to the ultrasonic instrument, and a processor including a control unit operably connected to the power source, the method includes: controlling supply of the electric energy to the ultrasonic instrument, obtaining a temperature value related to a temperature of the vibration transmission member, the vibration transmission member being separate from a transducer, and controlling the power source to reduce or stop the supply of electric energy of the power source based on the rate of change of the temperature value.

Abstract: Devices and methods for treating a target site in a body lumen are provided. A medical device includes a stent-like structure including a plurality of scoring and non-scoring filaments interwoven with one another. Generally, the stent-like structure will have more non-scoring filaments than scoring filaments to provide greater structural support and to focus the scoring forces on only a few select areas. The stent-like structure is expanded within the target site to score the target site and to provide temporary structural support while the target site is infused with a therapeutic agent. Such therapeutic agent infusion occurs with the use of a drug eluting or drug coated balloon disposed within the stent-like structure or by occluding the target site and introducing a drug into the occluded target site to sit for a period of time.

Abstract: A medical device includes a surgical needle attached to a hollow tubular suture. The suture is constructed of macroporous hollow tubular wall that facilitates and allows tissue integration into the suture core subsequent to introduction to the body, thereby preventing suture pull-through and improving biocompatibility.

Abstract: Provided is an endoscopic treatment tool including: a sheath that has a longitudinal axis; a first operation wire and a second operation wire that are inserted through the sheath so as to be able to be moved forward and backward; a treatment part constituted by a first wire rod and a second wire rod that have lower bending rigidity than bending rigidity of the second operation wire; a first joint part inside which the second wire rod passes and that joins a distal-end section of the first operation wire and a proximal-end section of the first wire rod; and a second joint part that joins a distal-end section of the second operation wire and a proximal-end section of the second wire rod.

Abstract: To provide a basket-type treatment instrument for an endoscope such that wires constituting a basket are not liable to be damaged. A basket-type treatment instrument 1 for an endoscope having a basket part 40 formed such that a plurality of basket wires 41, 42 elastically expand or contract radially, wherein folded-back parts 41a, 42a formed by folding back substantially center portions of the basket wires 41, 42 are hooked to a substantially cylindrical first rib 6b fixed in a perpendicular direction to the cylinder axis of a distal tip 6, whereby the distal tip 6 retains the distal sides of the basket wires 41, 42 together.

Abstract: Various embodiments of devices and methods of use are provided. The device can include a catheter shaft having a proximal end and a distal end. The device can include an extractor. The extractor can include engagement panels located at a first longitudinal location and engagement panels located at a second longitudinal location. The extractor can include a spacer between engagement panels located at the first longitudinal location and engagement panels located at the second longitudinal location. The device can include a sheath, wherein the extractor comprises a collapsed state within the sheath for delivery and an expanded state within a blood vessel. In the expanded state, the engagement panels are configured to engage material between engagement panels located at a first longitudinal location and engagement panels located at a second longitudinal location.

Abstract: A method for removing a clot from a vessel involves the use of a device that can have dual layers where an inner expandable member runs within an outer expandable member. The inner expandable member can be divided into one or more sections, with a proximal section having a clot pinching structure configured to pinch the clot between the pinching structure and an outer catheter. A distal flow channel section of the inner member can be configured to create a flow channel through the clot to restore blood to the downstream vasculature. The struts of the outer expandable member can form closed cells that are not fully circumferential in a proximal portion to allow a clot to pass inside and engage the pinching structure, and fully circumferential in a distal portion to scaffold the vessel for dislodging the clot. A protective element at the distal end of the device can prevent the escape of clot fragments.

Abstract: A handle assembly includes a drive wire coupled to an expandable end effector, the wire having a diameter of no more than 3 French and a handle cannula receiving the wire therethrough, rotation of the handle cannula transferring torque to rotate the wire. The assembly also includes a shaft receiving the handle cannula, rotation of the shaft transferring torque to rotate the handle cannula. The assembly further includes an actuation assembly receiving the shaft, the actuation assembly coupled to a sheath sized to receive the wire and end effector therethrough, the actuation assembly moveable between a proximal configuration in which the sheath is moved proximally to expand the end effector and a distal configuration in which the sheath is moved distally to retract the end effector, the actuation assembly including a rotation mechanism transferring torque to the shaft to rotate the shaft.

Abstract: A tissue anchor delivery device includes a handle, an elongate shaft extending from the handle, a pusher tube disposed at least partially within a lumen of the elongate shaft, a pusher hub coupled to the pusher tube, a needle disposed at least partially within a lumen of the pusher tube, a needle hub coupled to the needle, and an actuator configured to be fixed to the pusher hub and the needle hub. The actuator is further configured to advance the needle hub and the pusher hub a first distance, thereby causing a tip of the needle to protrude from a distal end of the elongate shaft, disengage from the needle hub, and advance the pusher hub a second distance relative to the needle hub, thereby causing a distal end of the pusher tube to advance over the needle and push a coiled suture form off of the needle.

Abstract: A cutting balloon catheter including a balloon mounted on a distal portion of a catheter shaft. The balloon includes a cutting member mounted on an exterior surface of the balloon which includes one or more features for providing the cutting member with enhanced flexibility for navigating tortuous anatomy and more closely conforms to the expansion characteristics of the balloon to which the cutting member is mounted.

Abstract: This document describes rotational atherectomy devices and systems for removing or reducing stenotic lesions in blood vessels by rotating an abrasive element within the vessel to partially or completely remove the stenotic lesion material.

Abstract: Provided is a tourniquet holder comprising a mounting base adapted to be operationally engaged with a handguard of an associated weapon, a first tang, a second tang, and an elongated retention strap. The mounting base has a substantially flat plate defining a first base face and a second base face, one or more fastener apertures, and one or more retention slots. The first tang extends in a direction substantially normal to the first base face. The second tang extends in a direction substantially normal to the first base face. The first tang and the second tang define therebetween a margin adapted to accommodate therein an associated tourniquet. The elongated retention strap passes through the one or more retention slots, has a first end and a second end that are selectably engagable with one another to define a loop adapted to retain therein the associated tourniquet.

Abstract: The present disclosure provides collapsible medical devices that may be introduced via a delivery device into a pre-existing patent foramen ovale or trans-septal puncture hole and left in place to provide both a sealing function on the atrial wall and a septal-access function for additional procedures. The disclosed medical devices include a penetrable and re-sealable gasket material disposed in an open lumen in the medical device. This penetrable and re-sealable material allows catheters or other medical devices to pass therethough for providing additional therapy to an individual. By allowing the access point or portal to be opened by a guidewire or another medical tool, the medical devices as disclosed herein may be particularly suitable for a variety of cardiac procedures including, for example, atrial fibrillation, mitral valve replacement or repair, left atrial appendage closures, and the like.

Abstract: Systems and methods can remove material of interest, including blood clots, from a body region, including but not limited to the circulatory system for the treatment of pulmonary embolism, deep vein thrombosis, cerebrovascular embolism, and other vascular occlusions. The capture system can include a tubular body comprising a first end, a second end, and an axial length therebetween, the first end having an opening and a capture guide. The capture system can include one or more tensioners coupled to the capture guide. The tubular body has a first configuration in which the first end and the capture guide are expanded while the second end and a majority of the tubular body remains compressed. The tubular body is transformable to a second configuration by application of tension by the tensioners. The catheter can remove a large volume of clot.

Abstract: An injection system for an intraocular lens (IOL) utilizes a folding device for the IOL. The folding device comprises a pair of co-acting winglets pivotable between an open position and a closed position, and together defining a hinge axis and a receptacle for the IOL. Each winglet has an outwardly extending, unitary leg portion defining a base plane that includes the hinge axis and a motion limiting protuberance on each said leg portion extending from the base plane. The base planes are situated at an angle relative to one another and the protuberances abut one another when the winglets are in the open position. The base planes merge into a single plane when the winglets are in the closed position.

Abstract: A stent graft system including a component having longitudinally extending outer surface and inner surface, the inner surface defining a lumen having a longitudinal axis, a plurality of stents distributed longitudinally along the component, and a plurality of suture loops, each suture loop attached to the inner outer surface, of the stent graft, a first suture loop spaced laterally and longitudinally relative to an adjacent suture loop when the component is in an expanded configuration, the plurality of suture loops aligned longitudinally along the stent graft when the stent graft is in a radially constricted configuration, at least one ligature having a proximal end and a distal end, the ligature extending through at least some of the plurality of suture loops, whereby tension on the at least one ligature longitudinally aligns the suture loops along the longitudinal axis of the component, thereby at least partially radially constricting the stent graft.

Abstract: The present teachings provide devices and methods of engaging, capturing, and retrieving emboli. Specifically, one aspect of the present teachings provides a device comprising a generally cylindrical body, with its proximal ends joining to a delivery system and a plurality of cells forming its luminal surface. The cylindrical body is configured to axially rotate as it radially expands. Another aspect of the present teachings provides a device comprising two elongated bodies one disposed within the other. As the device expands radially, both elongated bodies are configured to axially rotate independently.

Abstract: A medical device includes a handle with a proximal arm and a distal arm. The proximal arm and the distal arm are pivotable via a joint. The medical device also includes a tube coupled to the distal arm and a drive wire. A distal portion of the drive wire includes an expandable end effector. A portion of the drive wire is positioned within the tube, and a different portion of the drive wire extends proximally of the distal arm and is coupled to the proximal arm.