Abstract: An apparatus for supporting a medical device on a patient includes a mounting structure configured to be fitted onto the patient to encircle at least a portion of a body part of the patient. The mounting structure includes an inner layer and an outer layer that define a confinement. A jamming material is contained within the confinement. The jamming material is configured to flow within the confinement to conform to the shape of the body part of the patient onto which the mounting structure is fitted. The mass of jamming material is configured to harden and become rigid in its conformed shape in response to a vacuum being formed in the confinement.

Abstract: A fastening system and a deployment system for controlling translation and rotation of a deployment device are presented. A fastening system may comprise one or more components configured for arresting or restricting translation of a delivery catheter of a medical device, including a mitral valve fixation device such as the MitraClip®. A deployment system may comprise one or more components configured for locking rotation of a crimping cam to a slider to control deployment of a mitral valve fixation device.

Abstract: The devices and methods can provide short-term strength and rigidity and long-term stability and support after a bone and/or ligament injury in a single procedure. An orthopedic fixation device may include a body having a first end, a second end, and a length therebetween. The body may include a first portion, a second portion and a shaft portion disposed between the first portion and the second portion. The shaft portion may include one or more bioabsorbable materials. The body may include an internal channel disposed along the length. The device may also include a suture being disposed within the internal channel.

Abstract: A joint assembly for an endovascular device, comprising a shaft comprising a main body and an enlarged end, a proximal strut comprising a slot, wherein the slot engages the enlarged end of the shaft and a locking collar comprising a proximal face and a distal face, and at least partially covering the enlarged end of the shaft and the slot of the proximal strut, such that the locking collar constrains the proximal strut such that the proximal strut cannot disengage from the enlarged end of the shaft when the joint assembly and the clot retrieval device is under load.

Abstract: In the field of medicine and medical technology, improving the technical properties of endoprostheses used for the surgical treatment of hernias. A self-expanding mesh endoprosthesis for endoscopic hernioplasty includes a mesh fabric made of threads and a self-expanding system incorporated in the mesh fabric, wherein the self-expanding system is made of polyfilament titanium threads located both in the structure and along the contour of the endoprosthesis, and wherein the titanium threads of the mesh fabric are made with a relief surface. The technical result increases efficiency of performing laparoscopic hernioplasty operations, increasing the plasticity, and reducing the risk of breakage of the threads in the mesh structure, simplifying the surgical technique for passing through and placement of the endoprosthesis, reducing the duration and trauma of surgery and, accordingly, accelerating the recovery of patients.

Abstract: A device includes including an elongated hollow member with a window for receiving tissue in an interior of the hollow member; a rigid member slidably coupled to the hollow member; and an actuation mechanism configured to move the rigid member longitudinally along a longitudinal axis through at least part of the window. When a ligation band is adjacent to the window and the rigid member is moved relative to the hollow member, the rigid member deforms the ligation band from an open position into a closed position around tissue received in the window.

Abstract: Rotational atherectomy devices and systems can remove or reduce stenotic lesions in blood vessels by rotating an abrasive element within the vessel. The abrasive element can be attached to a distal portion of an elongate flexible drive shaft that extends from a handle assembly.

Abstract: A catheter delivery device for a self-expanding stent is described. The delivery device includes a distal catheter component and a distal sheath that releases the stent by moving proximally relative to the distal catheter component and the stent. A proximal catheter shaft including a tube and a pull wire within a lumen of the tube may be provided, the pull wire being attached to the distal sheath such that pulling the pull wire proximally relative to the tube pulls the distal sheath proximally to release the stent progressively. A casing tube may be provided to surround the catheter shaft, the casing tube having a distal end that receives telescopically a proximal end of the distal sheath. A method of making a delivery device for implantation of a self-expanding stent is also described.

Abstract: A stent device including a stent cover having differing porosity ratio is disclosed. The stent covers the stent body comprising of stent wires and stent cells enclosed by the stent wires. The stent cover differs in porosity ratio for areas covering the stent wires and the areas covering the stent cells. The porosity ratio for areas covering the stent wires may have a higher porosity rate in order to promote endothelialization of the stent device. A bilayer stent cover differing in porosity ratio may be used to cover the stent body, as well as stent cover not covering the entirety of the stent body.

Abstract: A flexible, elongated catheter tube having distal and proximal ends and a laser cut section there between. The laser cut section makes up a majority of the catheter length and is cut in a continuous helical pattern forming interlocking teeth which can be sinusoidal, triangular, square or like shapes, preferably sinusoidal. The interior of the tube has a polymeric layer which forms the internal lumen of the catheter. The exterior of the tube has a polymer coating. A short portion of the distal end is uncut and is followed by a narrower terminal section which can be tapered for better blockage penetration. The interlocking teeth disengage and reengage in a fish-scale manner without undergoing plastic deformation of the metal tube and without substantial polymer separation from the tube exterior.

Abstract: A catheter assembly may include a catheter hub and a catheter tube, which may extend distally from the catheter hub. The catheter assembly may include a push tab and one or more ribs extending outwardly from an upper portion of the catheter hub. The ribs may be shorter in height than the push tab and proximal to the push tab. A needle assembly may include a needle hub, an introducer needle extending distally from the needle hub and through the catheter tube, and a grip coupled to the needle hub. The grip may include a face disposed outwardly from the push tab and the ribs. A grip of a user may contact the push tab, the ribs, and the face to reduce rotation between the catheter hub and the needle hub in response to distal advancement of the catheter hub.

Abstract: Disclosed herein are catheter assemblies and methods thereof that address various aspects of at least the retrograde tunneling technique. The catheter assemblies include, but are not limited to, catheter assemblies configured for vascular access, catheter assemblies configured for priming, catheter assemblies configured for tunneling, and mechanisms for connecting catheter tubes to their respective catheter assemblies. The methods include, but are not limited to, priming, tunneling, and connecting catheter tubes to their respective catheter assemblies.

Abstract: A medical device comprises a catheter and an aspiration pump. The catheter has a hybrid reinforcement to improve performance characteristics. The aspiration pump is cycled to improve aspiration efficacy.

Abstract: A medical dispensing device which includes a catheter, an applicator tip at a distal end of the catheter, the catheter and the applicator tip defining a lumen having a longitudinal axis and a distal opening, a plunger in the lumen and movable along the longitudinal axis, and a plurality of elements in the lumen proximal to the distal opening and distal to the plunger, the plurality of elements stacked along the longitudinal axis for dispersement of one element at a time through the distal opening via a force applied by the plunger.

Abstract: A deflectable vascular catheter includes a proximal handle assembly, an elongated sheath extending distally from the proximal handle assembly and including a deflectable distal end portion, an actuation mechanism operatively associated within an interior cavity of the proximal handle assembly for deflecting the distal end portion of the sheath, an anchor ring located at a distal end of the deflectable distal end portion of the sheath, and a pull wire extending from the actuation mechanism to the anchor ring. The pull wire has a non-circular cross-section and is laser welded to an exterior surface of the anchoring ring.

Abstract: Syringe assemblies comprising a first cap and a second cap to ensure sterilization of the fluid path without the need for external packaging are described. Also described are methods of sterilizing the fluid path of a syringe assembly.

Abstract: A device for removing a protective shield such as a needle shield is disclosed. The device includes a cup shaped body with a sidewall, a distal bottom wall and a proximal opening. The protective shield is insertable into the cup shaped body through its proximal opening. Fingers are disposed opposite each other in openings in the sidewall. The fingers are flexibly coupled with the sidewall at a proximal end of the finger and can be resiliently biased inwardly to engage the protective shield. Each finger includes at least one projection for engaging the protective shield. The fingers may also include a distal engagement surface for engaging a lip on the protective shield.

Abstract: This invention relates to surgical suturing devices and methods by which suture may be passed through tissue during surgery, and, more particularly, to an improved blade of a suture passer needle. The suture passer needle includes a first side, a second side, and a blade disposed at an end of the needle. The blade has a first edge extending from the first side of the needle and a second edge extending from the second side of the needle, which converge to a tip of the blade. A notch is disposed in the blade and forms an opening in the first side of the blade. The blade also has one or more cutout portions distal and/or proximal the notch, which minimize the stress and strain placed on the blade. The suture passer needle can be incorporated into surgical suturing devices or suture passer devices to pass suture through a tissue body.

Abstract: In some examples, a catheter includes an elongated body and an expandable member at a distal portion of the elongated body and defining at least part of a distal tip of the catheter. The expandable member includes a flexible membrane and an expandable ring or partial ring located at a distal portion of the expandable member, wherein the expandable ring or partial ring is configured to expand radially outward in response to electrical energy applied to the expandable ring or partial ring.

Abstract: A pediatric catheter system may include a catheter adapter having a distal end, a proximal end, and a lumen extending therebetween. The lumen may include an upper surface and a lower surface with an adhesive coupled to the lower surface. The system may include a plurality of wings that extend outwardly from the catheter adapter. The plurality of wings may be configured to fold upwardly. The system may include a catheter cannula extending distally from the catheter adapter. The system may include a needle hub removably coupled to a proximal end of the catheter adapter and an introducer needle extending through the catheter tube. A proximal end of the introducer needle may be secured within the needle hub.