A surgical instrument end effector assembly includes a first jaw member defining an insulative tissue-contacting surface and first and second electrically-conductive tissue-contacting surfaces disposed on either side of the insulative surface. A second jaw member of the end effector assembly includes an ultrasonic blade body positioned to oppose the insulative surface of the first jaw member, and first and second electrically-conductive tissue-contacting surfaces disposed on either side of the ultrasonic blade body and positioned to oppose the first and second electrically-conductive surfaces, respectively, of the first jaw member. The first jaw member is movable relative to the second jaw member between a spaced-apart position and an approximated position to grasp tissue therebetween. The first and second electrically-conductive surfaces of the second jaw member are movable, independent of the first jaw member, relative to the first jaw member and the ultrasonic blade body between a retracted position and an extended position.

An esophageal ablation system including a positioner, an elongated, flexible shaft extending from the positioner, and a microwave emitter assembly disposed near the distal end of the shaft. The emitter assembly includes one or more microwave antennae and a balloon tor spacing the antennae relative to target tissue. The device may have an inner balloon for deploying the antenna. The systems, devices and methods disclosed are useful for treating Barrett's Esophagus, Esophageal Adenocarcinoma, and Squamous Cell Carcinoma.

An electrosurgical instrument (10) with two branches (11, 12) that are pivotably supported at each other by means of a pivot joint (13) is disclosed. The pivot joint (13) has a support pin (34) and a support cavity (37). The support pin (34) is particularly torque-proof connected with one of the branches (11) or (12) and rotatably supported in the support cavity (37) of the respective other branch (12) or (11). Between the branches (11, 12) a seal (45) is provided that sealingly abuts at the two branches (11, 12) and that surrounds the support pin (34) completely in the circumferential direction. Preferably, the support pin (34) is sealingly connected with the respective branch (11, 12) at its axial ends. In doing so, entering of contaminants in the area between the support pin (34) and the support cavity (37) from all sides or access possibilities is inhibited.

A surgical instrument includes a housing, a shaft extending therefrom, an end effector assembly supported by the shaft, a movable handle, and a drive assembly. The drive assembly includes a translatable drive member for actuating the end effector assembly, and a torsion spring including first and second legs. The first leg is configured to translate through the housing in response to movement of the movable handle relative to the housing. The second leg is configured to translate through the housing in cooperation with the first leg to move the drive member longitudinally when a force acting on the drive member is less than a threshold force, and to remain in fixed position, thereby tensioning the torsion spring and retaining the drive member in fixed position when the force acting on the drive member is equal to or exceeds the threshold force.

Some implementations include a coaxial bipolar ablation instrument comprising an outer needle and an inner needle inserted into the outer needle. The instrument can also include a first insulating layer disposed between the inner needle and the outer needle, and a second insulating layer disposed over a portion of the outer needle. The instrument can further include a first exposed region of the instrument disposed near a proximate end of the instrument, the first exposed region including a first exposed portion of the inner needle and a first exposed portion of the outer needle, the first exposed region constructed to provide contact to a connector, and a second exposed region of the instrument disposed near a distal end of the instrument, the second exposed region forming the active region of the instrument and including a second exposed portion of the inner needle and a second exposed portion of the outer needle.

Instruments having a hood that defines and surrounds a flow chamber. The flow chamber can serve for suction of emissions that are produced due to influence of an electrode supplied with high frequency voltage on biological tissue. For elimination of tissue deposition and other clogging from the flow chamber the electrode is surrounded by a movable hood that can be transitioned for cleaning purposes out of its operating position into a cleaning position.

A treatment system can include a treatment instrument with an operation input element that has a magnet; and a sensor that detects a parameter that changes with a movement of the magnet together with the operation input element based on an operation of the operation input element. The treatment system can also include a control apparatus that can control the supply of electrical energy to the treatment instrument for operation of the treatment instrument. The control apparatus includes a processor that can determine a relationship between a change in a distance between the sensor and the magnet and a change in the parameter, and to set, based on the relationship, a threshold for switching between an ON state and an OFF state of the supply of the electrical energy to the treatment instrument.

An end effector assembly of a forceps includes a first jaw with a tissue sealing surface and an electrode on the sealing surface, and a second jaw with a tissue sealing surface and an electrode on the sealing surface. The first jaw and the second jaw move between an open position and a closed position. The sealing surface of at least one of the first jaw and the second jaw has a rigid medial section and flexible lateral sections.

A microsurgical bipolar forceps may include an actuation structure, a hypodermic tube, a first electrical conductor, and a second electrical conductor. The actuation structure may include an actuation structure distal end, an actuation structure proximal end, and a plurality of actuation limbs. The hypodermic tube may be disposed in the actuation structure. The first electrical conductor may be disposed in the hypodermic tube and the actuation structure wherein the first electrical conductor is electrically connected to a bipolar cord. The second electrical conductor may be disposed in the hypodermic tube and the actuation structure wherein the second electrical conductor is electrically connected to the bipolar cord. A compression of the actuation structure may be configured to decrease a distance between a first jaw of the first electrical conductor and a second jaw of the second electrical conductor.

An electrode assembly (3) is provided for use in a resectoscope, the electrode assembly (3) comprising a pair of arms (4), and a tissue treatment element (9) depending from the arms. The arms (4) are pivotably mounted one to the other such that they are movable between a retracted position in which they lie alongside one another and a deployed position in which they diverge one from another. The electrode assembly (3) includes actuation means for moving the arms between their retracted and deployed positions. The tissue treatment element (9) is disposed at the distal end of each arm such that it is movable between at least two different operating positions.