Abstract: A medical instrument is disclosed having a structure capable of preventing liquid circulation between an inner layer side and an outer layer side of a peripheral wall portion. The medical instrument includes a main body portion in which a center hole and a radially outward space are partitioned by a tubular peripheral wall portion. The peripheral wall portion includes at least a first layer on which a hydrophilic member, in which a hydrophilic coating is formed on a first base portion, is disposed and a second layer on which a hydrophobic member, in which a hydrophobic coating is formed on a second base portion, is disposed. The peripheral wall portion is configured by the first layer and the second layer being stacked along a radial direction. As a result of swelling of the hydrophilic coating, the adjacent hydrophilic members come into contact with each other.

Abstract: Tissue fasteners carried on a tissue piercing deployment wire fasten tissue layers of a mammalian body together. The fasteners include a first member, a second member, and a connecting member extending between the first and second members. The first and second members are substantially parallel to each other. The fasteners may be deployed in limited spaces and in various applications including the restoration of a gastroesophageal flap valve.

Abstract: The disclosure relates to a needle-guiding device for a skin pricking device, comprising a base body, a skin pricking needle (3) and a needle channel (14), which is formed in the base body and in which the skin pricking needle (3) is arranged, wherein the skin pricking needle (3) can be moved back and forth repeatedly in the needle channel (14) along a movement path, wherein a channel wall (17) of the needle channel (14) has proximal guide wall sections (18) with respect to the skin pricking needle (3), on which the skin pricking needle (3) comes to rest for the needle guidance in response to the back and forth movement, and has distal wall sections (19), which are recessed relative to the proximal guide wall sections (18) and which are free from a direct contact with the skin pricking needle (3) in response to moving the skin pricking needle (3) back and forth in the needle channel (14). A skin pricker is furthermore provided.

Abstract: The present disclosure relates to the field of endovascular treatment. More particularly, the present invention uses a modified hydrogel intrasaccular occlusion device designed to implement an endovascular treatment to ameliorating or eliminating aneurysm recurrence, which hydrogel may optionally be impregnated with pharmaceutical compounds. The present invention also teaches the use of thin hydrogel coatings to ameliorate endovascular treatment related difficulties.

Abstract: An end effector for a surgical clip applier includes a housing, opposed first and second jaw members extending past a distal end of the housing and each comprising an independent structure movable relative to the other, a first cam track provided on the first jaw member and a second cam track provided on the second jaw member, and a cam providing first and second cam surfaces slidably engageable with the first and second cam tracks, respectively. A biasing device continuously urges the cam in a distal direction relative to the first and second jaw members, wherein the first and second cam surfaces and the first and second cam tracks are angled such that axial movement of the cam in the distal direction relative to the first and second jaw members causes the jaw members to close.

Abstract: There is provided herein, a device for treating and/or diagnosing a sinus or an ear condition, the device comprising a housing comprising or functionally connected to: a hollow cannula defining a lumen extending at least partially along the length thereof, the cannula is configured to be at least partially inserted through an ostium into a sinus cavity/ear of a subject; and a flexible grinding wire movable within the cannula's lumen and configured to be inserted into and retrieved out of the sinus cavity through the cannula's lumen, and to rotate along a longitudinal axis thereof and thereby grind, chop and/or stir material present in the sinus cavity and/or inside the hollow cannula, wherein the cannula is in fluid flow communication with an irrigation/aspiration source; and a wire handle functionally connected to the wire, allowing a user to advance and retrieve the wire within the cannula and into and out of the cannula lumen, wherein the device is handheld by a gripping handle.

Abstract: An implant delivery system comprises an elongate tubular member having a lumen, a tubular implant coaxially disposed within the lumen of the elongate tubular member, and a delivery assembly having a distal portion coaxially disposed within tubular implant. The delivery assembly comprises a delivery wire, an engaging bumper fixedly coupled to the delivery wire, a stopper bumper fixedly coupled to the delivery wire, and a floating element slidably coupled around the delivery wire and disposed between the bumpers, thereby limiting linear translation of the floating element therebetween. The floating element has an engaging portion configured to engage the engaging bumper when the delivery wire is axially translated relative to the elongate member in a first direction. The floating element is configured to radially expand outward to frictionally engage the implant when the engaging portion of the floating element engages the engaging bumper.

Abstract: Implants or systems of implants and methods apply a selected force vector or a selected combination of force vectors within or across the right atrium, which allow tricuspid valve leaflets to better coapt. The implants or systems of implants and methods make possible rapid deployment, facile endovascular delivery, and full intra-atrial retrievability. The implants or systems of implants and methods also make use of strong fluoroscopic landmarks. The implants or systems of implants and methods make use of an adjustable implant. The implants or systems of implants and methods may utilize a bridge stop to secure the implant.

Abstract: The present disclosure relates to heart valve prostheses, delivery devices, actuation handles, and other improved devices and methods that facilitate delivery of a heart valve prosthesis to a defective native valve structure in a patient, such as the aortic valve.

Abstract: A device for supporting an endoscopic tool may include opposite first and second arms extending along a first axis. An attachment system is configured to attach the first arm and the second arm to an endoscope. A curved guide for the endoscopic tool is coupled to the first arm, and has an outlet for launching the endoscopic tool. An angled tissue support surface is provided on the second arm, facing the outlet. The outlet is fixable in a working orientation relative to the first axis, and in the working orientation, a recess of the tissue support surface is configured to accept the endoscopic tool when launched from the outlet.

Abstract: The present invention provides a lifting member which easily inserts a medical thread into a muscle and induces the generation of an autogenous material. For example, the lifting member according to the present invention comprises: a needle having a through hole which is formed therein along the longitudinal direction; and a medical thread coupled to the outer circumference of the needle, wherein the medical thread may be finished to enwrap the end of the needle.

Abstract: Fixation device for engaging tissue including a pair of fixation elements, each fixation element has a first end and a second end opposite the first end, the first ends are moveable between a closed position and an open position. The fixation device further includes a pair of gripping elements. Each gripping element is moveable with a respective fixation element and disposed in opposition to at least a portion of the respective fixation element to capture tissue therebetween. The fixation device further includes a central portion operatively connected to each gripping element at a respective central portion-gripping element interface. The central portion has at least one distal end and a width “W1” proximate the distal end. Each of the gripping elements has a free end opposite its respective central portion-gripping element interface and a length “L1” defined between the respective central portion-gripping element interface and the free end.

Abstract: An instrument port for introducing instruments into a surgical site, including a port body having a channel running therethrough from a proximal end to a distal end, an instrument sleeve in slidable contact with the channel, creating a gap therebetween, and fluid flow for removing emboli efficiently from the instrument port, wherein the fluid flow includes the gap is provided. A fluid flow system for use in an instrument port is provided. A method of removably securing an instrument sleeve to a port body by anchoring the instrument port to heart tissue, making at least one flood line in a channel, flushing out emboli, and performing surgery with the instrument port.

Abstract: An introducer catheter device comprising a handle and an elongate shaft coupled to the handle and extending therefrom. The shaft defines a lumen therethrough, a longitudinal axis, and a first aperture in connection with the lumen. The shaft includes a movable deployment element configured for deploying an ancillary device from the first aperture at an angle relative to the longitudinal axis.

Abstract: Medical devices, medical device systems, and methods for making and using the same are disclosed. An example medical device may include an inner shaft having a stent receiving region. A bumper shaft may be disposed about the inner shaft. A deployment sheath may be slidably disposed about the inner shaft. The deployment sheath may have a body region and a distal stent covering region. The distal stent covering region may have an outer diameter that is smaller than an outer diameter of the body region.

Abstract: A reposable surgical clip applier is provided and includes a handle assembly, an endoscopic assembly selectively connectable to a housing of the handle assembly, and a clip cartridge assembly selectively loadable in and connectable to the endoscopic assembly.

Abstract: Retrieval of material from vessel lumens can be improved by electrically enhancing attachment of the material to the removal device. The removal device can have a core assembly that includes a hypotube coupled to a first electrical terminal and a pushwire coupled to a second electrical terminal, the pushwire extending through the hypotube lumen. An insulating layer separates the hypotube and the pushwire, and an interventional element is coupled to a distal end of the pushwire. The interventional element can be disposed adjacent to a thrombus. An electrical signal is delivered to the interventional element to promote adhesion of the thrombus to the interventional element. The electrical signal can optionally be a periodic waveform, and the total energy delivered can be between 0.75-24,000 mJ and the peak current delivered via the electrical signal can be between 0.5-5 mA.

Abstract: A handle assembly for a prosthesis delivery device is disclosed. The handle assembly has a proximal gripping portion and a stationary gripping portion. At least one rail extends distally from the proximal gripping portion through the stationary gripping portion. The proximal gripping portion is distally moveable along a longitudinal axis towards the stationary gripping portion from a first pre-deployment position to a second position. The at least one rail extends proximally from the stationary gripping portion when the proximal gripping portion is in a first pre-deployment position and distally from the stationary gripping portion when the proximal gripping portion is in a second position. The at least one rail is configured to prevent the build-up of torque along the length of the delivery device as well as prevent the build-up of torque among the various components of the handle assembly including the proximal gripping portion and the stationary gripping portion.

Abstract: An implant delivery system for delivering a sheet-like implant is disclosed. The implant delivery system includes a distal guidewire port for receiving the proximal end of guidewire after the guidewire distal end has been affixed to a first point on bone or other tissue. The implant delivery system is tracked over the guidewire to a selected position defined by the guidewire attachment. The device includes an implant spreader assembly disposed proximate the distal end of a delivery shaft. The implant spreader assembly includes a first arm and a second arm. The arms are coupled to the delivery shaft such that the first arm and second arm are moveable between a closed position and an open position. When pivoting to the open position the distal end of each arm travels in a generally transverse direction to spread a sheet-like implant.

Abstract: A surgical clip applier comprising a rotatable clip cartridge is disclosed. The surgical clip applier comprises a lockout that at least locks out the crimping drive of the surgical clip applier when the rotatable clip cartridge is empty.