Abstract: A surgical instrument includes a body, a shaft assembly, an end effector, a transducer assembly, and a loading assembly. The end effector is coupled with a distal end of the shaft assembly. The transducer assembly is removably coupled with the proximal end of the shaft assembly. The loading assembly comprises an actuator that is operable to couple the distal end of the transducer assembly with the proximal end of the shaft assembly. The loading assembly is operable to drive the transducer assembly through at least two stages of rotation to couple the distal end of the transducer assembly with the proximal end of the shaft assembly.

Abstract: A medical device including a medical device body that includes a first support structure, the medical device further comprising a first fixation anchor that includes a first anchor body extending between a first end and an opposing second end, and a hook portion extending from the first end, wherein the first anchor body engages the first support structure, and wherein the first fixation anchor is fabricated separate and apart from the medical device body. A method of making a medical device is disclosed.

Abstract: A banding apparatus and method. One embodiment is a unitary or integrated hemorrhoidal single hand-held and single hand-operated ligator, which can, in some embodiments, enable direct visualization and release of multiple bands. The ligator has a gun-shaped handle extending from a vacuum generating trigger tube, with a fixed band bearing barrel extending from the vacuum generating trigger tube. A vacuum generating tube extends through the band bearing barrel from the rear of the gun ligator to the band bearing barrel end of the ligator gun, and is in air movement communication with the vacuum generating tube and band bearing barrel end of the ligator gun. A band actuating barrel is threadably mounted to surround a portion of the band bearing barrel, and rotation of the barrel cause the barrel to move laterally and force one or more ligating bands along and off of the band bearing barrel end. A light source can be included to illuminate the band bearing barrel end.

Abstract: Devices, methods and systems are provided for occluding an opening within the tissue of a body, such as a left atrial appendage. In one embodiment, a system for use in occluding an opening in the tissue of a body includes a handle, a catheter coupled with the handle and a medical device disposed within a lumen of the catheter. The medical device includes an anchor system having a plurality of anchor segments coupled with an anchor hub. The medical device further includes an occluder system having a plurality of occluder segments coupled with an occluder hub. A first actuator is configured to displace the occluder hub independent of, and relative to, the anchor hub to deploy the occluder system from a refracted state to an expanded state while the anchor system remains in a retracted state.

Abstract: A combined multi-lumen central access catheter and an embolic filter including ports proximal and distal the filter for fluid infusion and/or pressure sensing and infusion ports in the catheter to permit infusion of bioactive agents, flushing agents and/or contrast agents. The embolic filter may be removably coupled to the multi-lumen catheter for temporary placement and retrieval under recommended indications.

Abstract: Devices, methods and systems are provided for occluding an opening within the tissue of a body, such as a left atrial appendage. In one embodiment, a medical device includes an occluder portion and an anchor portion, the anchor portion hingably coupled to the occluder portion. With this arrangement, the anchor portion actuates and pivots relative to the occluder portion between an anchor deployed position and an anchor non-deployed position while the occluder portion is in an occluder deployed position.

Abstract: A surgical instrument has a hollow tubular member, and a pressurization unit that has an outer valve portion, a pressurization device having a movable part configured to generate pressurized fluid when the movable part is moved, and an inner valve portion. The inner valve portion includes a first flow passage that is configured to fluidically connect a first port and a second port of the outer valve portion to each other when the inner valve portion is in a first position, and a second flow passage that is configured between the inner valve portion and the outer valve portion to fluidically connect the first port and a third port when the inner valve portion is in a second position. A sealing system fluidically isolates the second port and the third port from each other at any position of the inner valve portion.

Abstract: An insertion portion rigidity changeable catheter with a balloon has an insertion portion including a coil-shaped member which is extensible and contractible, with a compression length set to be a predetermined length, and a sheath which is a tube body with flexibility having a fluid conduit, includes a sheath main body surrounded by the coil-shaped member, and a sheath end portion provided at one end side of the sheath main body, and having a contact surface which one end surface of the coil-shaped member contacts, has one opening of the fluid conduit in the sheath end portion and has another opening of the fluid conduit at another end side of the sheath main body, an inflatable/deflatable balloon which is inflated by being supplied with a fluid via the one opening of the fluid conduit to expand to a diameter larger than an outside diameter of the sheath end portion, and is deflated by the fluid being discharged via the one opening to be brought into close contact with an outer circumferential face of the sh

Abstract: Embodiments of a clamping system are disclosed. In some embodiments, a system used with a motor assembly and a clamping device is presented, the system adjusting torque limits in the motor assembly according to conditions, for example operating temperature of the motor assembly and aging of the clamping device and the motor assembly. The clamping device can be, for example, a stapler or a vessel sealer.

Abstract: A deployment system for vascular repair of a transected body vessel is provided. The system can include a prosthesis, an inner sheath, and an outer sheath. The inner sheath can be configured to selectively retain a first portion of the prosthesis in the compressed configuration, leaving a remaining portion of the prosthesis uncovered by the inner sheath. The outer sheath can be configured to retain the remaining portion of prosthesis in the compressed configuration and the first portion of the prosthesis within the inner sheath. The outer sheath is removable from the prosthesis to allow an expansion of the remaining portion of the prosthesis to the expanded configuration at a first opening in the transected vessel. The inner sheath is removable from the prosthesis first portion to allow an independent expansion of the first portion to the expanded configuration at a second opening in the transected vessel.

Abstract: A wound closure device includes a shaft, a sleeve, a suture, and a cartridge. The sleeve is disposed about the shaft and defines first and second sleeve arms movable between a retracted position, wherein the sleeve arms extend along the shaft, and a deployed position, wherein the sleeve arms extend outwardly from the shaft. The cartridge includes a base and first and second cartridge arms. The base is configured for releasable coupling with the shaft and defining a pocket configured to retain an intermediate portion of the suture. The first and second cartridge arms are configured for positioning adjacent the respective first and second sleeve arms and are configured to move in conjunction with the respective first and second sleeve arms between the retracted and deployed positions. The first and second cartridge arms are configured to retain first and second ends of the suture, respectively.

Abstract: The invention provides a device (50) and system for treating a heart valve having an anchor (54, 56) and one or more sutures attached to the anchor. The anchor has an expanded deployed configuration and a low caliber undeployed configuration. A delivery in a heart includes catheter and a needle slidable in the lumen of the catheter. The distal end of the catheter is inserted through the myocardium of the heart until the catheter tip is juxtaposed to the underside of the valve leaflet to be treated. The leaflet is then pierced with tip of the needle. The needle is pushed until the anchor in its undeployed configuration passes through the needle tip and is released from the catheter. The anchor is then brought to its deployed configuration on one or both surfaces of the valve leaflet.

Abstract: Devices, methods and systems are provided for occluding an opening within the tissue of a body, such as a left atrial appendage. In one embodiment, a medical device coupled to a delivery catheter includes a fluid flow path that facilitates contrast fluid to pass through the delivery catheter and the medical device to a distal side thereof to provide imaging information as to the position of the medical device positioned in the opening, such as the left atrial appendage. In another embodiment, a medical device is coupled to a delivery catheter, the medical device including flaps adjacent a hub of the medical device that close-off a bore of the hub upon the catheter being detached from the medical device.

Abstract: A medical device may include an elongate member including a proximal end and a distal end. The medical device may also include a rotatable member at the distal end of the elongate member. The rotatable member may be rotatably coupled to the distal end of the elongate member. The rotatable member may include a longitudinal axis, and may be configured to rotate about the longitudinal axis. The rotatable member may also include a gripping element configured to engage a layer of tissue. The gripping element may be configured to selectively couple at least a portion of the layer of tissue to a surface of the rotatable member, to restrict relative movement between the portion of the layer of tissue and the surface of the rotatable member, during rotation of the rotatable member.

Abstract: Novel cerebral vasculature devices are disclosed, including thrombectomy removal devices that include a continuous braided structure, a proximal portion, a distal portion, and a first expandable portion located between the proximal portion and the distal portion. The braided structure includes a plurality of wires. The proximal portion and the distal portion include polymer imbedded at least partially into the braided structure. The device is useful for removing thrombus from a patient's vasculature.

Abstract: Suture tracking dilators and methods for removing implanted medical devices such as microstimulators or microsensors from living tissue are described. A suture tracking dilator has a slit running along its axial length. The slit can have a curved portion. A suture is attached to a medical device prior to its implantation. To remove the implanted medical device, the free end of the suture is exposed and inserted in the slit in the suture tracking dilator. The suture is held under tension at its free end, the dilator is inserted in the living tissue and the dilator follows the suture to the implanted medical device. The medical device is removed by pulling on the free end of the suture.

Abstract: A lancer device that enables a user to draw blood from a patient and discard the used lancet without touching it. The device also has an adjustable tip for selecting the depth of stylet penetration into the patient and a triggering mechanism that utilizes a yoke latch and a leaf spring to discharge the lancet. The lancer also has a dampening feature to reduce vibrations when the lancet is moving.

Abstract: The apparatus has a delivery shaft 30 bearing a tubular device constrained within a moveable sheath 36, and a handle comprising a hollow shaft 124 with a static grip 126 and a grip slider 122 movable proximally or distally. The grip slider is connected to a slider block 24 fixed to a sheath hub 6 to which the sheath is fastened. A retraction wheel 120 has a spool 2 for winding a retraction wire 121 connected to a retraction block 20 in contact with the slider block enabling the slider block to be pushed as the retraction block is retracted distally. Initial incremental movement of the retraction block by winding of the retraction wire, moves the slider block and retraction block simultaneously. Subsequently the slider block is movable independently of the retraction block using the grip slider, leaving the retraction block behind.

Abstract: A stocking for a compression-therapy patient comprises a foot portion matingly removably receiving and surrounding a foot. A closable/openable leg portion extends from the foot portion, removably receives a leg, defines adjoining edges of the leg portion, and includes a band defining an uppermost area of the leg portion and material of which is more compressive/supportive than a remainder thereof. A fastening device extends along the leg portion and continuously fastens/unfastens the edges to/from each other and closes/opens the leg portion such that the stocking can secure and apply continuous pressure to the foot/leg. The device includes a zipper and an enfoldment connected and secured along a continuous inner edge of the zipper, including material that is different than the band and/or remainder of the leg portion, and disposed between the zipper and skin and contacting the skin such that the enfoldment prevents the zipper from contacting the skin.

Abstract: Featured is a medical instrument driver, a robotic apparatus embodying such a medical instrument driver and methods related thereto for inserting a medical instrument into tissue of a mammal (e.g., human). Such medical instruments include medical needles, biopsy needles, trocars, cutters and introducers. Such a medical instrument driver according to the present invention is configured and arranged so that medical instrument is rotated as it is being moved longitudinally for insertion into the tissue such that the medical instrument is spiraling as it pierces and traverses the tissue to the target area.