A surgical instrument includes an elongated shaft including an articulating segment. A jaw assembly extends from a distal segment of the elongated shaft. A first jaw member can be actuated between a closed configuration and an open configuration. An articulation cable assembly includes a first articulation cable including a first extending portion, a second extending portion spaced apart from the first extending portion, and a loop portion connecting distal ends of the first and second extending portions of the first articulation cable. A first ferrule is positioned about the loop portion of the first articulation cable. A second articulation cable includes a first extending portion, a second extending portion spaced apart from the first extending portion, and a loop portion connecting distal ends of the first and second extending portions of the second articulation cable. A second ferrule is positioned about the loop portion of the second articulation cable.

Introducers for detachably coupling with an ablation probe are described herein. The ablation probe can be a cryoablation probe or other type of ablation probe such as microwave or RF ablation probe. An example introducer includes a hollow member; and a locking mechanism configured to secure the introducer and the ablation probe. An example system includes an ablation probe; and an introducer that is configured to detachably couple with the ablation probe. The introducer includes a hollow member, one or more energy elements arranged along an axial direction of the hollow member, and one or more sensor elements arranged along the axial direction of the hollow member.

A bipolar-microscissor forceps assembly includes a forceps having a first forceps arm having a first forceps distal tip and a first forceps proximal end and a second forceps arm having a second forceps distal tip and a second forceps proximal end. The second forceps proximal end is connected to the first forceps proximal end. A microscissors is disposed between the first forceps arm and the second forceps arm. A kit with a plurality of microscissors releasably connected to the forceps is also provided.

A knife configured for use with an electrosurgical forceps having curved jaw members and a method of manufacturing the same. The knife includes a distal body having an inner side and an outer side, a first etching on the outer side of the distal body defining a distal cutting edge and a second etching on the outer side of the distal body extending along a portion of a length of the distal body to define relatively protruded and relatively recessed surfaces extending along a portion of the length of the distal body on the outer side thereof.

Devices, systems and methods are provided for subdermal tissue tightening through soft tissue coagulation and for use in cosmetic surgery applications. The devices, systems and methods of the present disclosure may be used for a minimally invasive application of helium-based cold plasma energy to subcutaneous tissue for the purpose of tightening lax tissue. In various aspects of the present disclosure, distal tips, each including at least one port for applying plasma to patient tissue are provided for use with an electrosurgical apparatus.

Proposed is a smoke pencil with swivel device, in which first end portions of first and second cases are rotatably coupled to a body and second end portions of the first case and the second case are inclined downward, so when a user rotates the body, a cable and a suction hose are guided downward. Accordingly, there is an effect that a user can easily rotate the body.

An arthroscopy system includes both a motorized handpiece and a detachable probe. The motorized handpiece includes a rotating driver which is configured to engage a rotatable drive coupling within a hub of the probe. The probe has a shaft with an articulating distal region, and the rotatable drive coupling is configured to convert the rotary motion of the rotating driver to an articulating motion within the articulating region of the probe.

Tissue modification instruments. In some embodiments, the instrument may comprise a shaft extending along an axis. A tissue treatment tip may be positioned at a distal end of the shaft. The tissue treatment tip may comprise one or more energy delivery elements configured to deliver tissue-modification energy. The tissue treatment tip may comprise a non-branching tip that extends away from the axis to define a tissue treatment region that is wider than a width of the shaft. The tissue treatment tip may comprise a terminal end, which may be positioned at the distal end of the instrument in some embodiments or may be positioned proximal of the distal end of the instrument.

An apparatus includes a body, a catheter, and a fluid connector assembly. The catheter extends distally from the body and includes at least one electrode and at least one irrigation port. A fluid conduit is in fluid communication with the at least one irrigation port. A fluid connector assembly extends proximally from the body and includes a fluid connector body and a grounding member. The fluid connector body is configured to couple with a complementary connector associated with a fluid source. A proximal end of the fluid conduit is positioned in an interior region of the fluid connector body. The grounding member is interposed between the proximal end of the fluid conduit and the fluid connector body. The grounding member is in communication with the interior region of the fluid connector body such that the grounding member provides an electrical ground to fluid communicated to the fluid conduit via the fluid connector body.

A method of treating tissue of a patient uses a device including a mother case, a belt, at least one treatment unit and at least two applicators. The treatment method may include attaching first and second applicators to the belt at a working distance to the patient's surface, and providing different treatment energy to the first applicator and the second applicator. A treatment pattern is created by the applicators providing the different treatment energies. The hardware pattern or positions of the applicators on the belt may be changed before and/or during the treatment. The hardware pattern may be based on selected treatment effect and body part.