Abstract: A system for compressing body tissue including a clip having first and second tissue compressing surfaces. The clip is movable from a closed position to an open position wherein the clip receives tissue between the first and second tissue compressing surfaces to compress tissue between the first and second tissue compressing surfaces. A clip deployment device has a first clip engagement member and a second clip engagement member engageable with the clip, the first and second clip engagement members movable between first and second positions to controllably move the clip.

Abstract: A surgical instrument includes a selectively rotatable housing, an adaptor, and a shaft including an end effector. The adaptor is coupled to the housing and is selectively movable between a first position and a second position. The shaft is coupled to one or both of the housing and the adaptor. The end effector is articulable in response to the selective rotation of the housing. The end effector is articulable toward a first direction when the adaptor is positioned in the first position and articulable toward a second direction when the adaptor is positioned in the second position. The first and second directions are different.

Abstract: A surgical instrument includes a selectively rotatable housing, an adaptor, and a shaft including an end effector. The adaptor is coupled to the housing and is selectively movable between a first position and a second position. The shaft is coupled to one or both of the housing and the adaptor. The end effector is articulable in response to the selective rotation of the housing. The end effector is articulable toward a first direction when the adaptor is positioned in the first position and articulable toward a second direction when the adaptor is positioned in the second position. The first and second directions are different.

Abstract: A surgical instrument includes a selectively rotatable housing, an adaptor, and a shaft including an end effector. The adaptor is coupled to the housing and is selectively movable between a first position and a second position. The shaft is coupled to one or both of the housing and the adaptor. The end effector is articulable in response to the selective rotation of the housing. The end effector is articulable toward a first direction when the adaptor is positioned in the first position and articulable toward a second direction when the adaptor is positioned in the second position. The first and second directions are different.

Abstract: A surgical device for performing surgery includes a handle assembly, an elongate member extending from the handle assembly, an articulation mechanism, and an adapter. The elongate member has articulating and straight sections. The articulating section is configured to articulate with respect to the straight section. The adapter rotatably couples the elongate member with the articulation mechanism such that when the elongate member is in a first rotational orientation with respect to the articulation mechanism, the articulating section articulates toward a first direction relative to the straight section upon movement of the handle assembly towards the first direction with respect to the straight section and when the elongate member is in a second rotational orientation with respect to the articulation mechanism, the articulating section articulates toward a second direction relative to the straight section upon movement of the handle assembly towards the first direction with respect to the straight section.

Abstract: A surgical instrument includes a selectively rotatable housing, an adaptor, and a shaft including an end effector. The adaptor is coupled to the housing and is selectively movable between a first position and a second position. The shaft is coupled to one or both of the housing and the adaptor. The end effector is articulable in response to the selective rotation of the housing. The end effector is articulable toward a first direction when the adaptor is positioned in the first position and articulable toward a second direction when the adaptor is positioned in the second position. The first and second directions are different.

Abstract: Vessel wound closure systems and method for sealing a puncture wound in a target vessel, such as those puncture wounds that occur from interventional procedures. The vessel wound closure system comprises at least a biocompatible, viscoelastic, self-sealing septum material injected onto the adventitia of the target vessel prior to performance of an interventional procedure. The prior injected septum material remains and seals the puncture wound of the target vessel even after various components associated with accessing the target vessel and the performance of the interventional procedure are removed from the target vessel and the puncture wound.

Abstract: A surgical instrument includes a selectively rotatable housing, an adaptor, and a shaft including an end effector. The adaptor is coupled to the housing and is selectively movable between a first position and a second position. The shaft is coupled to one or both of the housing and the adaptor. The end effector is articulable in response to the selective rotation of the housing. The end effector is articulable toward a first direction when the adaptor is positioned in the first position and articulable toward a second direction when the adaptor is positioned in the second position. The first and second directions are different.

Abstract: A surgical device for performing surgery includes a handle assembly, an elongate member extending from the handle assembly, an articulation mechanism, and an adapter. The elongate member has articulating and straight sections. The articulating section is configured to articulate with respect to the straight section. The adapter rotatably couples the elongate member with the articulation mechanism such that when the elongate member is in a first rotational orientation with respect to the articulation mechanism, the articulating section articulates toward a first direction relative to the straight section upon movement of the handle assembly towards the first direction with respect to the straight section and when the elongate member is in a second rotational orientation with respect to the articulation mechanism, the articulating section articulates toward a second direction relative to the straight section upon movement of the handle assembly towards the first direction with respect to the straight section.

Abstract: A surgical instrument includes a selectively rotatable housing, an adaptor, and a shaft including an end effector. The adaptor is coupled to the housing and is selectively movable between a first position and a second position. The shaft is coupled to one or both of the housing and the adaptor. The end effector is articulable in response to the selective rotation of the housing. The end effector is articulable toward a first direction when the adaptor is positioned in the first position and articulable toward a second direction when the adaptor is positioned in the second position. The first and second directions are different.

Abstract: A fixed needle syringe has a syringe barrel with its distal portion modified to accept a needle protective housing. In particular, the distal portion is formed with the a groove dimensioned to accept a collar that is attached to the housing. The inside surface of the collar is provided with a number of flanges that fit within the groove formed at the distal portion of the syringe barrel of the fixed needle syringe. Protrusions are provided at the inside surface of the collar to frictionally act against the syringe barrel, so that the needle protective housing does not freely rotate, but is rotatable relative to the syringe barrel by the application of a predetermined torque to either the collar or the housing attached thereto. An internal hook is provided in the housing to grasp the needle of the syringe, when the housing is pivoted to cover the needle extending from the needle hub of the syringe.

Abstract: Vessel wound closure systems and method for sealing a puncture wound in a target vessel, such as those puncture wounds that occur from interventional procedures. The vessel wound closure system comprises at least a biocompatible, viscoelastic, self-sealing septum material injected onto the adventitia of the target vessel prior to performance of an interventional procedure. The prior injected septum material remains and seals the puncture wound of the target vessel even after various components associated with accessing the target vessel and the performance of the interventional procedure are removed from the target vessel and the puncture wound.

Abstract: A sterilization device which causes occlusion to the fallopian tubes of a patient is designed to be trancervically positioned in the intramural portion of the tube without perforating the tube. The device includes a flexible hollow catheter having an interior passageway, a distal end for insertion trancervically into a patient, and a proximal end opposite the distal end for grasping and manipulation by a physician. The device further includes a pair of diametrically opposed electrodes, each being movably mounted on the distal end of the catheter and radially movable with respect to the distal end.

Abstract: A sterilization device which causes occlusion to the fallopian tubes of a patient is designed to be trancervically positioned in the intramural portion of the tube without perforating the tube. The device includes a flexible hollow catheter having an interior passageway, a distal end for insertion trancervically into a patient, and a proximal end opposite the distal end for grasping and manipulation by a physician. The device further includes a pair of diametrically opposed electrodes, each being movably mounted on the distal end of the catheter and radially movable with respect to the distal end.

Abstract: An electrosurgical instrument and method is provided for transecting an organ. The electrosurgical instrument includes an introducer having a channel therein, and a conductive wire positioned in and deployable from the channel. A deployment device on the introducer is capable of moving the conductive wire between an undeployed position wherein it is substantially positioned within the channel, and a deployed position wherein a portion is deployed from and positioned outside of the channel and has a substantially looped configuration. A capture element at the distal end of the introducer can secure the distal end of the wire to the introducer, and the deployment device can subsequently move the wire toward the undeployed position to thereby cinch the conductive wire.

Abstract: A fixed needle syringe has a syringe barrel with its distal portion modified to accept a needle protective housing. In particular, the distal portion is formed with the a groove dimensioned to accept a collar that is attached to the housing. The inside surface of the collar is provided with a number of flanges that fit within the groove formed at the distal portion of the syringe barrel of the fixed needle syringe. Protrusions are provided at the inside surface of the collar to frictionally act against the syringe barrel, so that the needle protective housing does not freely rotate, but is rotatable relative to the syringe barrel by the application of a predetermined torque to either the collar or the housing attached thereto. An internal hook is provided in the housing to grasp the needle of the syringe, when the housing is pivoted to cover the needle extending from the needle hub of the syringe.