835 results about "Suture needles" patented technology

An apparatus and a method for surgical suturing with thread management. An apparatus for tissue suturing comprising a cartridge having a suturing needle having a pointed end and a blunt end, the suturing needle capable of rotating about an axis; a pusher assembly comprising a cartridge holder having a needle rotation drive capable of releasably engaging the cartridge and rotating the suturing needle about the axis; and an actuator capable of releasably engaging the needle rotation drive to rotate the needle rotation drive. A method for suturing tissue comprising placing a suturing device having a cartridge containing a suturing needle to span separated tissue segments; activating an actuator to cause rotational movement of the suturing needle through the separated tissue segments; and deactivating the actuator to stop an advancing movement of the suturing needle to cause a suturing material to be pulled through the separated tissue segments forming a stitch.

A semi-robotic apparatus and methods of use thereof for suturing body tissue, wherein the apparatus includes a housing; at least two distal arms connected to and extending distally from the housing, wherein the at least two distal arms are independently both extendable and retractable; a suture needle clasp connected to a distal end of each of the at least two distal arms, wherein the suture needle clasp is radially rotateable orthogonal to the longitudinal axis of the distal arm to which it is connected; and at least one controller operable for controlling at least a portion of the extension or retraction of the at least two distal arms, the rotation of the suture clasps and the opening and closing of the suture needle clasps.

An implantable port with an integral attachment mechanism. The implantable port includes one or more suture needles enclosed within a port body, the suture needle(s) coupled to a movable member such that movement of the movable member results in movement of the suture needle(s) out of the port body and into the tissue of a body into which it is implanted. The movable member can be a cam or tensioning member that rotates about a central port axis. The movable member can be coupled to a gear to permit movement of the movable member following implantation of the port within a subcutaneous pocket.

When closing the sternum in cardiothoracic surgery, elderly people with a fragile sternum can experience bleeding from the suture sites because of loose knots. The knots are loose because of the danger of cutting into the sternum from the tension caused by the suture wire. In extreme cases, the sternum can be fractured. If the closure is attempted intercostally, there are internal thoracic arteries that run longitudinally underneath the sternum and they may be hurt if a sharp needle is used. Intercostal fixation on its own is inadequate, and additional wires that directly insert into the manubrium are required. Of the sternal closure wires currently available, there is discordance in the numbers provided and actually used, resulting in leftovers that need unnecessary sterilization and reuse. To solve the above problems, an intercostal specific blunt needle has been devised, and packaged together with a sharp needle that will directly insert into the sternum. The set may contain one of each needle or a required combination of both, and come in a pre-sterilized pack. The needle is blunt at the cutting edge, and has a hook, or a side hole. The opposite end has a handle attached. The needle is configured so the wire can be hooked on, or threaded through the hook and hole respectively, and the operative procedure involves lifting up the wires.

Improved medical suturing devices, systems, and methods may hold a suture needle at a fixed location relative to a handle of the device, allowing the surgeon to grasp and manipulate the handle of the suturing device to insert the needle through tissues in a manner analogous to use of a standard needle gripper. Cycling the handle from a closed position to an open position and back to the closed position may alternate the device between gripping the needle with a first clamp (for example, along a proximal portion of the needle) to gripping the needle with a second clamp (for example, along a distal portion of the needle) and optionally back to gripping with the first clamp, with the needle often staying at a substantially fixed location relative to the suturing device body. Related single-clamp needle grasping devices can be bent plastically by a surgeon, and/or have bodies that are grasped by a hand while a portion of the hand actuates a handle.

A ring or rings adapted for endoluminal placement within the stomach, other hollow organ or vessel, and a method for deploying the rings is described. The rings create a small pouch with a reinforced stoma in the stomach for the treatment and control of obesity. An endoluminal suturing device for deploying a circumferential line of interrupted mattress suture bites is inserted into the patient's stomach via the patient's mouth. The distal gastric ring is preloaded on the distal end of the suturing device and is incorporated with suture loops from the double-armed sutures contained within the device. The suturing device can have an expandable area at its distal end that can expand its diameter to between approximately 10 mm and 150 mm. The circumference of this expanded area has a suction opening that is used to draw in tissue when a vacuum is applied to the device. Flexible cannulas containing long flexible suture needles are positioned radially around the circumference of the suction opening. The long needles are are adapted to be advanced through the drawn in tissue incorporating their attached suture material. The expandable area of the device is collapsed, and the device is withdrawn from the patient. With the distal ring anchoring the sutures beneath the incorporated tissue folds, a column of sutures exits the device's suction port as the device is withdrawn. A second, proximal ring is then incorporated with the sutures and may then be endoscopically lowered into the patient's stomach and positioned proximal to the distal ring. The sutures are endoscopically secured and cut, thereby fixing the two rings together with tissue incorporated between them.

Apparatus for needle grasping and performing a second modality comprising a sheath axially extending between distal and proximal ends thereof. The device includes an inner hollow tube with a slot formed therein for receiving a needle at the distal end. Retraction and extension of the inner tubular member relative to the sheath enable the grasping and releasing of a suture needle received in the slot. A handle is provided at the proximal end of the apparatus for selectively extending and retracting the inner tube relative to the sheath and for retaining the inner tube in its extended and retracted positions. A second switch can be provided in the handle to actuate a catheter slidably inserted through the inner tube to perform a second therapeutic modality. The catheter preferably includes a distal bight that forms a loop when extended from the distal end of the sheath for facilitating intracorporeal knot tying thereat. The catheter includes a lumen therethrough for receiving suture thread for use at the distal end of the sheath.

The invention provides a multifunctional suture needle that may be used to draw a suture through tissue surrounding a wound while simultaneously delivering a bioactive fluid through the needle tip. The suture needle possesses an internal cavity capable of containing a fluid, and a fine aperture adjacent to the point of the needle through which the fluid may egress. The fluid may be driven from the needle through the needle tip with a compressed gas that is sealed within the cavity adjacent to the fluid. Alternatively a fluid conducting suture may be employed to deliver fluid through the internal passage of the suture needle and out the aperture adjacent to the tip of the needle. The rate at which the fluid is emitted from the suture needle may be controlled by carefully selecting the fluid viscosity, design of the needle or suture passages, and pressure applied to the fluid.

An endoscopic suture needle and related surgical endoscopic suturing devices are to be used in conjunction with an endoscope. The invention relates to suturing of internal body tissue as part of a surgical procedure which may be diagnostic, therapeutic or both. In accordance with the present invention, there is provided an endoscopic surgery system comprising a temperature biased suture needle, a needle grasping device, and an elongated catheter or other delivery tube, a endoscopic surgery system configured for use in conjunction with a flexible or rigid endoscope insertion member.

A guard attachable to a forceps is provided. In one embodiment, the guard is releasably securable to one arm of the forceps. In another embodiment, the guard is permanently secured to or integral with one arm of the forceps. In another embodiment, the guard is rotatable with respect to the forceps. A barrier portion of the guard extends between the forceps' arms, or along an outside of the forceps' arms. The barrier prevents tissue from getting between the forceps' arms. A physician can thus use the barrier to displace tissue from a surgical site. The barrier also provides protection to surrounding tissue, preventing suturing needles from pricking the tissue behind the barrier or pricking the physician. The guard may be slidable along at least a portion of the length of the forceps.

A vascular suturing device is disclosed which includes an elongated tubular body defining opposed proximal and distal end portions and having a longitudinal axis extending therethrough, the body including an inner tubular member, an outer tubular member and a central tubular member disposed between the inner and outer tubular members. The inner tubular member and the central tubular member are mounted for movement relative to the outer tubular member about the longitudinal axis of the body for sequentially driving a pair of suture needles through the wall of a blood vessel to close an incision formed therein. A vascular dilator having a tapered distal tip portion is supported within the inner tubular member and is dimensioned to extend beyond the distal end of the inner tubular member for positioning the suturing device at the incision in the wall of the blood vessel. The dilator is configured to direct blood flow from the distal portion of the dilator to a location remote from the blood vessel for observation to confirm the location of the device.

An arthroscopic meniscal tear repair device comprises a catch needle and a transfer needle. which are pierced into a torn meniscus and advanced past the tear. Suture is transferred by a suture needle from the transfer needle through the meniscus and into the catch needle. The catch needle has an internal mechanism that retains the suture. The suture needle is then retracted back to its home position inside the transfer needle, leaving the free end of the suture across the meniscus and in the catch needle. The device is then retracted out of the meniscus, leaving behind a stitch across the meniscal tear inside the meniscus. A pre-tied knot of suture is then slid down the device and cinched up using a knot pusher having a dilation tip, thus completing the repair.

A prosthetic implantable device that offers a reduction in fluid loss when the device is punctured, such as by a dialysis needle or suture needle, and the needle is subsequently removed. The device may be made to be thin and flexible, and with longitudinal stretch, in order that it also offers good handling and kink resistance to a surgeon. While the device is preferably of tubular form, flat sheets or other forms may also be made. The device includes inner and outer layers of a porous material having a microstructure of nodes interconnected by bent fibrils, and having void spaces between adjacent bent fibrils. The inner and outer layers are joined by an elastomeric adhesive that may interpenetrate the void spaces of the adjacent surfaces of the inner and outer layers, that is, the inner surface of the outer layer and the outer surface of the inner layer. Optionally, a middle layer of an elastomeric material may also be provided, joined to the inner and outer porous layers by the interpenetrating elastomeric adhesive. The device is preferably a vascular graft and more preferably a vascular graft for kidney dialysis.

A suture needle is disclosed that includes a shaft, the shaft being marked at least partially with a visual indicator; and a puncture tip at one end of the shaft. The shaft of the needle includes a front surface and a rear surface. The front and/or rear surface of the needle includes the visual indicator. The visual indicator may be a color, but if both the front and rear surfaces include a color, then the colors of front and rear surfaces are different. Also disclosed are methods of using a suture needles, one such method including: inserting the suture needle into a mammal; viewing the suture needle; and immediately ascertaining the exact orientation of the suture needle with no manipulation of the suture needle.

Improved medical suturing devices, systems, and methods may hold a suture needle at a fixed location relative to a handle of the device, allowing a surgeon to grasp and manipulate the handle of the suturing device to insert the needle through tissues. The exemplary device includes two needle grasping clamps extending from an elongate distal portion for endoscopic surgeries, including ear, nose and throat procedures. The two clamps alternate holding the suture needle, as the surgeon sutures the tissues, each clamp having a proximal and distal gripping jaw for grasping the needle. Preferably, the gripping surfaces of the proximal and distal gripping jaws are substantially parallel to the needle's plane of curvature and exert a holding force on the needle substantially along an axis of the device.

Suture needles are a significant safety hazard for medical workers, mainly because of accidental needlestick injuries. Disclosed herein are safety suture needle assemblies and related methods. In particular, variations of a safety suture needle having an activatable sheath or flexible extension member are disclosed. The implementation of certain embodiments of the disclosed invention can result in a desired improvement in safety, including the prevention of unwanted needle punctures, while achieving efficient suturing.