Abstract: A rivet, rivet introduction device, and method therefor. The rivet is configured for deployment from a rivet introduction device to provide for connection of tissue. The rivet preferably includes two expansion zones configured to secure tissue therebetween, with the expansion zones being either self-expanding or expandable by use of a mandrel. The rivet introduction device preferably is configured to provide for introduction of a rivet with access only to one side of the tissue to be connected.

Abstract: Suture Locks, as well as related systems and methods, are provided for fixing strands of one or more sutures relative to tissue. The suture locks, systems and methods are simple and reliable in use, facilitate complete perforation closure and adjustment of the suture strands, and are adaptable to a variety of suture fixation and perforation closure situations. The suture lock includes a locking pin and a retaining sleeve. The locking pin has a main body and a grip. The retaining sleeve has a tubular body with an internal wall defining an internal passageway sized to receive the locking pin therein. The suture lock is operable between a locked configuration and unlocked configuration. In the locked configuration, the suture strands are compressed between the grip and the internal wall of the tubular body.

Abstract: Medical devices, systems and methods for placing tissue fixation devices are provided. The medical device includes a plurality of elongate delivery devices, a plurality of elongate tubes, and a distal tip. Each delivery device defines a delivery lumen sized to receive a tissue fixation device. Each elongate tube defines a tube lumen sized to receive one of the delivery devices. Each tube lumen has a distal port. The distal tip is connected to the plurality of elongate tubes and defines a guide surface positioned distally of the distal ports. The guide surface is structured to redirect the plurality of delivery devices radially outwardly as the plurality of delivery devices are distally translated through the tube lumens and the distal ports of the plurality of elongate tubes. A medical system is formed by an endoscope that is selectively attachable to the medical device.

Abstract: An endoscopic assembly for an endoscope is disclosed. The assembly comprises a ligator barrel having proximal and distal portions. The proximal portion has a seat and a receiving wall extending to a proximal end. The receiving wall has a first threaded portion formed thereon. The assembly further comprises a connector for connecting the ligator barrel about the endoscope. The connector has a scope portion and a tip portion. The scope portion has a receiving end through which the endoscope is disposed to engage the seat for connecting the ligator barrel about the endoscope. The tip portion has a second threaded portion formed thereon and are configured to cooperate with the first threaded portion to receive the receiving wall and attach the connector with the ligator barrel. The first and second threaded portions are configured to cooperate with each other to tighten the connection of the ligator barrel about the endoscope as the threads increase surface area contact therebetween.

Abstract: Medical devices and methods for the treatment of obesity. The medical devices generally include an attachment portion for attaching the medical devices on or adjacent the pylorus and a limitation portion for limiting the passage of stomach contents through the pylorus to delay emptying the stomach. The limitation portion may be responsive to pressure from stomach contents to substantially close or to open the passageway.

Abstract: Medical devices and methods are provided for forming an intestinal bypass anastomosis, such as for treatment of obesity. The medical devices and methods are minimally invasive and reduce complications. Two magnet assemblies are deployed in a spaced apart relationship, and are transluminally brought together to approximate the tissue and form an anastomosis therebetween.

Abstract: Medical devices and related methods for closing a perforation in a bodily wall The medical device generally includes a suture having opposing first and second ends and a set of visceral anchors. Each visceral anchor includes a crossbar having opposing ends and a suture slidably attached thereto. Each visceral anchor is passed through the bodily wall adjacent the periphery of the perforation. The ends of the suture are tensioned to reduce the distance between the visceral anchors and compress the bodily wall around the perforation. The ends of the suture are secured to maintain the compression of the bodily wall and close the perforation.

Abstract: An elongate medical device configured for navigation through a lumen is provided. The device includes an elongate shaft having a proximal portion and a distal portion. The distal portion includes a first interlocking connector. The device further includes a loop portion operably connected to the distal portion. The loop portion includes a second interlocking connector configured for connecting to the first interlocking connector. A medical system is also provided including a catheter and a wire guide. A method of making a wire guide is provided.

Abstract: A medical system for approximating the esophageal sacs in an infant afflicted with esophageal atresia. The medical device includes an esophageal catheter and a gastric catheter. The distal end of the esophageal catheter, which includes a magnetic tip, is passed through the esophagus to the upper esophageal sac. The distal end of the gastric catheter, which also includes a magnetic tip, is passed through a gastrostomy and into the lower esophageal sac. The magnetic forces created by both magnets results in approximation of the esophageal sacs. Pressure-induced necrosis establishes a passageway between the esophageal sacs. A stent or stent-graft can be deployed within the established passageway to prevent re-synopsis of the esophagus.

Abstract: A device for directing a wire guide into a bodily passageway such as a branch of the biliary tree or other difficult to access bodily passageway. The device includes a member, such as an inflatable balloon or a self-expanding basket, for obstructing a first passage. Once the balloon is inflated, or the basket expanded, the wire guide can be reliably directed or deflected into a preferred adjacent passageway in order to cannulate the preferred adjacent passageway. A procedure for cannulating a preferred passageway by obstructing a passageway in the natural flow-path of a wire guide is also provided.

Abstract: A clip device for hemostasis includes an introducing tube (outer sheath) insertable into a body cavity. An operating wire is slidably inserted into an inner sheath, which in turn is separately advanceable and retractable within the outer sheath (introducing tube). The operating wire has a distal end portion and a retainer attached to the distal end portion of the operating wire. The clip device further includes a clip having a proximal end portion and at least three arm portions extending from the proximal end portion and provided with a tendency to open. A first retainer is attached to the distal end of the clip and is matingly received by a second retainer provided on the operating wire. A clip sliding ring is provided for closing the arm portions of the clip. Methods for delivering the clip and for causing hemostasis are also provided.

Abstract: An apparatus and method comprising at least one intragastric member or artificial bezoar made of a digestive-resistant or substantially indigestible material that is introduced into a gastric lumen of a mammal for the treatment of obesity. The intragastric member or artificial bezoar is typically at inserted into the gastric lumen in a partially compacted configuration, whereby it is then manipulated into, or allowed to assume, a second expanded configuration sufficiently large to remain within the reservoir of the stomach during normal activities and not be passed through the pylorus into the intestines. In animals, the present invention has been found to be effective in achieving weight loss over a several month period, while being easy to place and retrieve.

Abstract: A clip device for hemostasis includes an introducing tube (outer sheath) insertable into a body cavity. An operating wire is slidably inserted into an inner sheath, which in turn is separately advanceable and retractable within the outer sheath (introducing tube). The operating wire has a distal end portion and a retainer attached to the distal end portion of the operating wire. The clip device further includes a clip having a proximal end portion and at least three arm portions extending from the proximal end portion and provided with a tendency to open. A first retainer is attached to the distal end of the clip and is matingly received by a second retainer provided on the operating wire. A clip sliding ring is provided for closing the arm portions of the clip. Methods for delivering the clip and for causing hemostasis are also provided.

Abstract: A device for directing a wire guide into a bodily passageway such as a branch of the biliary tree or other difficult to access bodily passageway. The device includes a member, such as an inflatable balloon or a self-expanding basket, for obstructing a first passage. Once the balloon is inflated, or the basket expanded, the wire guide can be reliably directed or deflected into a preferred adjacent passageway in order to cannulate the preferred adjacent passageway. A procedure for cannulating a preferred passageway by obstructing a passageway in the natural flow-path of a wire guide is also provided.

Abstract: An apparatus and method comprising at least one intragastric member or artificial bezoar made of a digestive-resistant or substantially indigestible material that is introduced into a gastric lumen of a mammal for the treatment of obesity. The intragastric member or artificial bezoar is typically at inserted into the gastric lumen in a partially compacted configuration, whereby it is then manipulated into, or allowed to assume, a second expanded configuration sufficiently large to remain within the reservoir of the stomach during normal activities and not be passed through the pylorus into the intestines. In animals, the present invention has been found to be effective in achieving weight loss over a several month period, while being easy to place and retrieve.