Abstract: A clip unit including: a clip main body having a first arm portion, a second arm portion, and a middle portion; a pressing tube formed in a tube shape to be capable of accommodating the clip main body, the pressing tube being provided to deform the clip main body so as to make a distal end of the first arm portion and a distal end of the second arm portion to approach to each other, as the middle portion, the first arm portion, and the second arm portion are moved toward a proximal end side of the clip unit; a locking portion configured to protrude from an inner circumferential surface of the pressing tube on the proximal end side of the pressing tube; and a first locked portion configured to protrude from a lateral surface of the first arm portion.

Abstract: The present invention provides a tourniquet apparatus that can be inflated hands-free. The tourniquet apparatus includes a sleeve and a pressurizing device to provide pressurized air to inflate the sleeve as required. In the tourniquet apparatus, the pressurizing device includes a pedal that is foot-operated and can be used to regulate the flow of pressurized air therein.

Abstract: The invention relates to a suturing device used to place sutures inside the human body during various medical procedures. The suturing device includes an elongate body member, a needle deployment mechanism and a needle receiving portion. The elongate body member has a distal portion that defines an opening. The needle deployment mechanism is disposed at least partially within the elongate body member for moving a needle out of the opening at the distal portion of the elongate body member into a tissue; and the needle receiving portion is provided at the distal portion of the elongate body member to capture the needle. The needle receiving portion has a non-planar surface with walls that are non-parallel with respect to a longitudinal direction of the needle receiving portion such that the walls converge to form an aperture formed in the needle receiving portion to receive the needle.

Abstract: A surgical instrument includes a housing, an end effector, a movable handle, and a drive assembly. The movable handle includes first and second cantilever spring arms and is movable relative to the housing between a spaced-apart position and an approximated position. The first cantilever spring arm is flexed upon movement of the movable handle from the spaced-apart position towards the approximated position to bias the movable handle towards the spaced-apart position. The drive assembly is operably coupled between the movable handle and the end effector such that movement of the movable handle from the spaced-apart position towards the approximated position moves the end effector from an open position towards a clamping position for clamping tissue. The second cantilever spring arm is flexed upon application of a threshold pressure to tissue clamped by the end effector to control an amount of pressure applied to tissue clamped by the end effector.

Abstract: An inserter device that has a driver, a removable inserter tip (or plurality of inserter tips) and a cannulation device slidable over the inserter tip is provided, wherein the removable inserter tip is provided as an interchangeable component of the device, one configuration of the interchangeable inserter tip being of a substantially hexagonal cross-sectional shape (suitable for accommodating a screw-in fixation device (screw), and another configuration of the interchangeable inserter tip being of a substantially circular cross-sectional shape (suitable for accommodating a push-in anchor). A suture anchor assembly has the inserter device that is used with a plug-in anchor, a screw-in anchor, or interchangeably with a plug-in or screw-in anchor, is also disclosed. A method for assembling the suture anchor assembly as well as a method of using the surgical assembly for tissue repair are also provided.

Abstract: The present invention provides an eye marker tip that includes a base, one or more marking wings, and a marking element attached to a marking wing and configured to deliver ink (or another indicator) to a surface of an eye. Embodiments may include a hollow or translucent post and light channel, or a base having a fixation button, to form a central light shape visible to a patient. Embodiments may include either or both of a magnifying lens and a parabolic light deflector, to form circles of light that may be used in connection with a central light shape to properly align the eye marker tip with a patient's eye.

Abstract: A system for passing suture through biological tissue using a cannula, introducer or other minimally invasive means, to approximate, ligate, fixate and/or close biological tissue. The system includes a hand grip in operative communication with an elongated tubular member having a jaw mechanism disposed on the tubular member distal end. The elongated tubular member housing a deformable tubular needle therein having a curvilinear portion and an internal lumen. The jaw mechanism includes a needle shield that is configured to deflect and flex when the tubular member is slidably translated into the needle shield.

Abstract: A system for controlling a relationship between first and second bodies and made up of a suture assembly with at least a first suture configured to define a restrictable loop structure with the suture assembly in an operative state. At least first and second restrictable sub-loops cooperatively define a first loop that can be reduced in size to thereby produce a force on the first and second bodies that urges them towards each other. A first loop length has a first sliding portion with a second loop length having a second sliding portion. At least one knot extends around the first and second sliding portions. The first and second sliding portions, upon each being moved within the at least one knot in a tightening sliding direction, cause a size of a respective sub-loop to be reduced.

Abstract: The methods and devices disclosed herein promote temporal control of balloon inflation patterns. The devices include a covering for a portion of the balloon that compresses the balloon portion during the inflation process. This enables the distal portion of a balloon to be inflated prior to the proximal portion of a balloon, creating a tapered shape at lower inflation pressures. This is especially useful during transvascular implantation procedures, as it prevents dislodgement of an implant mounted on the balloon. As inflation continues, pressure exerted on the balloon by the covering is overcome such that the proximal region of the balloon inflates, forming a shape with generally straighter sides than the tapered shape, thereby expanding the cardiovascular device.

Abstract: A self-stabilizing pneumatic abdominal aortic tourniquet that utilizes a semi-ridge retaining strap, a ratcheting retaining buckle, and an elastic guide cord on the lower penetrating end of a wedge-shaped bladder. A rigid baseplate is supported by a waist belt having a width identical with the waist belt so that the baseplate provides a stable base for positioning the bladder over a selected area of the patient's abdomen. The air bladder is affixed to the underside of the baseplate, which is initially kept in a deflated condition collapsed against the baseplate, and includes an elastic cord, such as a shock cord, configured to bias the tip of the wedge or “V” shaped bladder in the middle of the baseplate. An air source connected to the air bladder causes inflation and penetration of the lower edge of the bladder into the patient's abdomen thereby causing aorta occlusion.

Abstract: A medical suture needle made of stainless steel includes a cutting blade component and a body part continuing to the cutting blade component. The cutting blade component, whose degree of thickness decreases from the body part to a sharp point, includes a first cutting blade part and a second cutting blade part continuing from the first cutting blade part. The first cutting blade part includes two first slanted surfaces formed sandwiching an apex and a first bottom surface sandwiched by the two first slanted surfaces. Cutting blades are formed at an edge constituting the apex and at edges where the first bottom surface and the two first slanted surfaces intersect. The second cutting blade part includes first slanted surfaces, second slanted surfaces having rims approximately parallel to the apex and formed on the respective first slanted surfaces, and a second bottom surface sandwiched by the second slanted surfaces.

Abstract: Methods and apparatus for a percutaneous bypass graft system according to various aspects of the present technology include a graft section comprising a dual-sided fixation system at the anastomosis site and a tamper sheath configured to provide enhanced control during installation. The dual-sided fixation system may comprise a plurality of barbs configured to secure the graft section to an internal and external portion of a target vessel. The tamper sheath comprises a cuff at a distal end that is configured to be positioned against an outer surface of the target vessel during the percutaneous procedure.

Abstract: An obstruction removal device is described, having one or more engaging members which can engage portions of the clot. The one or more engaging members have a collapsed, delivery state, and an expanded, deployed state.

Abstract: A medical device includes (a) a capsule including a lumen extending therethrough, a proximal end of the capsule including at least one window extending therethrough; (b) a bushing including a channel extending therethrough, a distal end including at least one arm extending distally therefrom such that a corresponding one of the arms is releasably engagable with a corresponding one of the windows; and (c) a core member including a locking portion and at least one engaging element. The locking portion is sized and shaped to be received within the channel of the bushing to apply a pressure to the arm such that the arm engages the windows. The engaging element extends laterally outward from a portion of the core member such that the engaging element engages a corresponding one of the arms to deform the arms radially inward and out of engagement with the windows.

Abstract: A tissue anchor includes a plate having a top surface and a bottom surface, and an array of first pins coupled with the plate, whereby each first pin includes an elongated shaft having a lower end with a first barb facing away from the bottom surface of the plate. The plate has an array of second pin apertures that are offset from the first pins, whereby each second pin aperture has a diameter that extends from the top surface to the bottom surface of the plate. The tissue anchor includes an array of second pins extending through the second pin apertures, whereby each second pin has an elongated shaft having an upper end including a second barb facing away from the top surface of the plate and a lower end including a stop that is located below the bottom surface of the plate. The elongated shafts of the second pins have outer diameters that are smaller than the diameters of the second pin apertures for allowing the elongated shafts of the second pins to slide within the second pin apertures.

Abstract: In accordance with invention an application device for nasal splints is created, comprising at least one hollow body for accommodating a nasal splint, and a plunger which can be moved within the hollow body, wherein one end face of the hollow body is open so that a nasal splint contained in the hollow body can be introduced through a movement of the plunger from the hollow body through the open end face into the nose of a patient.

Abstract: A medical device may include a sheath, an elongate member at least partially surrounded by the sheath, an end effector at a distal end of the elongate member and movable between an open position and a closed position, and a handle. The handle may include an actuator member coupled to the sheath, an adjustment member, and a biasing member extending between the actuator member and the adjustment member.

Abstract: A dilation catheter system is provided to dilate the ostium of a paranasal sinus or some other anatomical passageway (e.g., within the ear, nose, or throat, etc.). The system may include a dilation catheter, a dilator, a guide catheter, and an inflator. The dilation catheter may be positioned between the dilator and the inflator. The guide catheter is configured to guide the dilator into the affected passageway. The inflator may then be actuated to transfer fluid from the inflator, through the dilation catheter, and into the dilator. The transfer of fluid may inflate the dilator to an expanded state to open or dilate the affected passageway. The inflator may include a body, a plunger assembly, and locking features that selectively secure the position of the plunger assembly relative to the body by moving along a path that is transverse to a longitudinal axis defined by the plunger assembly.

Abstract: A surgical instrument includes a shaft and a tissue fastener. The tissue fastener is releasably attached to the distal end portion of the shaft. The shaft is operable to rotatably drive the tissue fastener about a longitudinal axis of the shaft. The tissue fastener includes a base, first and second arms, and barbs. The first and second arms extend laterally and longitudinally from the base and are configured to be received within a first and second tissue portion, respectively. The first and second arms are configured to draw the first tissue portion against the second tissue portion. The barbs extend from the first and second arms and are configured to anchor the first and second arms within the first and second tissue portions. The shaft is configured to release the tissue fastener thereby securing the first tissue portion against the second tissue portion with the tissue fastener anchored therein.

Abstract: A surgical apparatus includes a debriding device, a hollow tube, and an irrigation assembly. The debriding device is fitted at a distal end of the surgical apparatus and is configured to debride tissue from a debriding site in a patient body. The hollow tube is configured to evacuate the debrided tissue away from the debriding site. The irrigation assembly is configured to apply irrigation fluid, via one or more orifices formed in the hollow tube, to the debrided tissue being evacuated.