Abstract: The present embodiments provide medical apparatuses, systems, and methods for rapidly forming an anastomosis between two viscera. The medical apparatus generally comprises two bases with two clamp members rotatably attached to the bases, the clamp members being capable of compressing tissue. The system generally comprises positioning and then deploying the medical apparatus between and within two stomas via an elongate member. The method generally comprises using the medical system to create an anastomosis between the stomach and the jejunum.

Abstract: The present embodiments provide systems and methods suitable for delivering a therapeutic agent to a target site. The systems generally comprise a container for holding a therapeutic agent, and a pressure source configured to be placed in selective fluid communication with at least a portion of a reservoir of the container. In one embodiment, fluid from the pressure source is directed through a first region of the container in a direction towards a second region of the container. The fluid then is at least partially redirected to urge the therapeutic agent in a direction from the second region of the container towards the first region of the container and subsequently towards the target site. In alternative embodiments, the fluid from the pressure source may be directed through the second region of the container in a direction towards the first region of the container.

Abstract: The present embodiments provide systems and methods for repairing tissue using one or more tacking devices. In one embodiment, the system comprises a graft member and at least one protective member configured to enclose at least a portion of a tacking device. The protective member may include, without limitation, a pocket having an enclosure forming an interior space, a plug of material or a barrier layer. When at least one tacking device is deployed to couple the graft member to the tissue, at least a portion of the tacking device is enclosed by the protective member to reduce the exposure of the tacking device.

Abstract: Embodiments include a fiducial deployment system and method for use thereof. A fiducial may include one or more protuberances configured to engage one or more slots in a needle of the system. The needle may be configured to deliver a plurality of fiducials to a target location in serial fashion, one at a time. In certain embodiments, echogenic placement of fiducials may present certain advantages.

Abstract: Medical devices, systems and related methods for delivering a plurality of tissue anchors. The medical devices generally comprise a needle and an over-the-needle suture lock, employed via inner and outer sheaths. The medical systems include a plurality of tissue anchors and at least one biodegradable or resorbable spacer member positioned between adjacent tissue anchors in conjunction with the medical devices.

Abstract: Medical devices and related methods for closing a perforation in a bodily wall The medical device generally includes a set of tissue anchors and an elongate tensioning member. Each anchor includes a crossbar having opposing ends and defining a longitudinal axis. A strand is connected to the crossbar at a location between the opposing ends and projects away from the longitudinal axis. The stand includes a distal end connected to the crossbar and a proximal end having a first connector. The elongate tensioning member is structured to selectively engage and disengage the first connector. The strands of the anchor are capable of being tensioned and fixed together for closing the perforation. The tensioning member is removed after the strands are fixed together.

Abstract: The present invention provides a wire guide (20) suitable for use in a body vessel, such as a peripheral vessel. The wire guide comprises a core member (22) and a first coiled member (40), each having proximal and distal ends. In one embodiment, the core member comprises at least one recessed portion (36), wherein the proximal end of the first coiled member is seated at least partially within the recessed portion to form a substantially flush exterior surface with the core member. The wire guide further preferably comprises a second coiled member (50) having proximal and distal ends, wherein the second coiled member is disposed distal to the first coiled member. The distal end of the first coiled member may be partially intertwined with the proximal end of. the second coiled member. A shaping ribbon (60) may be disposed substantially beneath the second coiled member to achieve a desired curvature at the distal tip of the wire guide.

Abstract: Multi-luminal endoscopic systems for sterilely delivering deployable devices or obtaining bodily tissues. The system comprise an outer catheter comprising a wall that encloses an outer lumen; an inner catheter movably disposed within the outer lumen and having an inner lumen; a balloon-tipped catheter movably disposed within the inner lumen and having a distal end and a proximal end, wherein the distal end of the balloon-tipped catheter comprises a balloon tip that can be expanded to contact the wall of the outer catheter to provide a seal to prevent bodily fluids from entering the outer lumen; and a push catheter having a lumen and is located within the outer lumen. The delivery systems can comprise concentric catheters. Systems used for tissue collecting can comprise catheters with different common center.

Abstract: A magnetic retraction device is provided that may be used to manipulate organs and tissue. The device includes a magnetic agent, at least one inflatable member configured to contain the magnetic agent, and a magnetic device. The inflatable member can be disposed on an elongate member adapted for delivery into a patient lumen. The inflatable member can be interconnected with one or more additional inflatable members by a sling.

Abstract: The present embodiments provide apparatus and methods suitable for containing and delivering a therapeutic agent to a target site. The apparatus generally comprises at least one container for holding a therapeutic agent, and a pressure source for facilitating delivery of the therapeutic agent. In one embodiment, the pressure source may be placed in selective fluid communication with a proximal region of the container and fluid from the pressure source may flow through at least a portion of the container to urge the therapeutic agent through the container towards the target site. In an alternative embodiment, the pressure source may be selectively in fluid communication with either a first hollow tube and the container so that therapeutic agent is urged into a catheter, or with a second hollow tube and a catheter so that a fluid from the pressure source bypasses the container and enters the catheter.

Abstract: An electrosurgical cutting device and method thereof for incising tissue are disclosed. The electrosurgical cutting device includes an asymmetrical cutting element that is affixed to a distal end of a torque cable. The cutting element is disposed within an end cap and is axially movable between a retracted position and an extended position. Rotation of the torque cable during a procedure allows the cutting element to rotationally align with and hook the target tissue onto the cutting element. An elongate member of the cutting element selectively lifts the target tissue away from surrounding tissue and structures. Having lifted the tissue away the surrounding tissue and structures, incision can occur.

Abstract: Medical devices for attaching suture to tissue and that provides reliable and complete closure of perforations and increases the versatility of the device for various other procedures. Embodiments of the medicals devices include a tissue anchor having a crossbar with opposing ends and structure for slidably receiving a suture.

Abstract: A cytology device and a method of use thereof are described. The cytology scraper comprises a scraping element that provides increased tissue removal capabilities over conventional cytology brushes. The edges of the scraping element can also simultaneously dilate strictures during the tissue removal procedure.

Abstract: A medical device and a method of using such medical device for removing targeted tissue from a body lumen in a patient is presented. The method generally comprises placing the distal end of the device through a natural orifice in the patient to a location that is proximate to the targeted tissue; deploying a T-anchor fastened to a suture strand through the targeted tissue; deploying a loop anchor into the tissue of the body lumen spaced away from the targeted tissue, whereas the suture strand is slidably received by the loop anchor; applying tension to the suture strand; cutting the tissue at a predetermined depth around the periphery of the targeted tissue; and removing the targeted tissue along with the T-anchor from the body lumen. The tension applied to the targeted tissue maintains the targeted tissue in a raised position and/or allows the physician to manipulate the targeted tissue relative to the tissue that is proximate to it.

Abstract: Medical devices and related methods are provided for treating a bleeding side of an internal bodily organ that are robust and versatile for use in a variety of endoscope applications. One embodiment of a medical device includes a catheter, a sheet and elongated forceps. The catheter defines a catheter lumen and is sized to be received within the accessory channel of the endoscope. The sheet is formed of hemostatic fabric formed into a tubular configuration having opposing first and second ends. The elongated forceps have a pair of collapsible grasping jaws. The grasping jaws are collapsed around the first end of the sheet, and the grasping jaws and sheet are received within the catheter lumen.

Abstract: Described herein are a system and a method for forming a stent of a desired length endoluminally. The system includes an elongate stent body and an outer sheath overlying the stent body. An endoluminal cutting mechanism is operatively connected to a drive cable in communication with the outer sheath. The cutting mechanism is configured to cut the stent body in response to motion of the drive cable. The method of forming the stent of a desired length endoluminally includes directing a system including an elongate stent body and an outer sheath overlying the stent body into a body lumen, positioning the stent body at an endoluminal site, and severing the stent body to form a stent of a desired length at the endoluminal site. An undeployed portion of the stent body remains in the outer sheath for optional deployment in a subsequent severing operation.

Abstract: A method and device for incising tissue within the gastrointestinal tract is described. The device is an electrosurgical sphincterotome cutting device. The sphinctertome includes a pre-curved, heat set FEP distal tip. An electrically conductive cutting wire is positioned along the pre-curved distal tip. Manipulating a control handle tightens the cutting wire and incises and cauterizes target tissue. The curvature of the distal tip allows the sphincterotome to orient and steer itself towards a patient's sphincter as it emerges from an accessory channel of an endoscope.

Abstract: The present embodiments provide apparatus and methods suitable for delivering a therapeutic agent to a target site. The apparatus generally comprises at least one container for holding a therapeutic agent, and a pressure source for facilitating delivery of the therapeutic agent. In one embodiment, the pressure source may be placed in selective fluid communication with a proximal region of the container and fluid from the pressure source may flow through at least a portion of the container to urge the therapeutic agent through container towards the target site. In an alternative embodiment, the container and the pressure source may be coupled to first and second inlet ports of a connecting member, respectively, such that the therapeutic agent flows through an outlet port of the connecting member and towards the target site.

Abstract: A medical device and method for its use in the digestive system of a mammalian patient is provided. The medical device includes a stent and a retrieval device. The stent has a magnetic element connected to an end of the stent. The retrieval device includes a magnetic member, and the retrieval device is sized to be ingested by the patient. The magnetic member is capable of being magnetically coupled to the magnetic element of the stent for removal of the stent through the natural forces of the digestive system.

Abstract: Described herein are a system and a method for forming a stent of a desired length endoluminally. The system includes an elongate stent body and an outer sheath overlying the stent body. An endoluminal cutting mechanism is operatively connected to a drive cable in communication with the outer sheath. The cutting mechanism is configured to cut the stent body in response to motion of the drive cable. The method of forming the stent of a desired length endoluminally includes directing a system including an elongate stent body and an outer sheath overlying the stent body into a body lumen, positioning the stent body at an endoluminal site, and severing the stent body to form a stent of a desired length at the endoluminal site. An undeployed portion of the stent body remains in the outer sheath for optional deployment in a subsequent severing operation.