In known electrosurgical handheld devices, a strengthening tube is firmly connected to a working element or a main body. Before the strengthening tube is connected to the main body, a contact body has to be pushed over the strengthening tube. For this purpose, the contact body has a corresponding bore. When the contact body is replaced for maintenance reasons or because of defects, the strengthening tube has to be removed with difficulty from the main body in order to be able to withdraw the contact body from same. The invention makes available an electrosurgical handheld device and a contact body which is able to be manipulated and maintained in a particularly simple and also time-efficient manner. This is achieved by the fact that a contact body for an electrosurgical handheld device has a slit parallel to a continuous bore and also parallel to a longitudinal axis of the handheld device.

A method of manufacturing an end effector for a surgical instrument includes providing a substrate wherein at least an outer periphery of the substrate is formed from an electrically-insulative material. The method further includes forming at least one ridge on the outer periphery of the substrate and depositing an electrically-conductive material onto the at least one ridge to form at least one electrode.

Spinal tumor ablation devices and related systems and methods are disclosed. Some spinal tumor ablation devices include electrodes that are fixedly offset from one another. Some spinal tumor ablation devices include a thermal energy delivery probe that has at least one temperature sensor coupled thereto. The position of the at least one temperature sensor relative to other components of the spinal tumor ablation device may be controlled by adjusting the position of the thermal energy delivery probe in some spinal tumor ablation devices. Some spinal tumor ablation devices are configured to facilitate the delivery of a cement through a utility channel of the device.

The limiting device includes a clamping portion and a movable portion; the clamping portion and the movable portion are both annular structures, two ends of the clamping portion and the movable portion are respectively connected to form a connected double-ring structure, and the ring diameter of the movable portion is larger than that of the clamping portion. The limiting device is disposed on a core rod, the clamping portion and the core rod are in interference fit, and the movable portion and the core rod are in clearance fit. When the movable portion cooperates with the core rod, the limiting device may slide relative to the core rod; when the clamping portion cooperates with the core rod, the limiting device and the core rod are in a fixed state, and the limiting device cannot slide relative to the core rod, thus achieving the purpose of limiting.

A forceps having at least a first jaw with a longitudinal axis is disclosed. The first jaw can include a body portion, a first flange, a second flange and a cam pin. The first flange can define a first cam slot with a longitudinal extent along the longitudinal axis. The second flange can be spaced from the first flange a distance transverse to the longitudinal axis of the first jaw and can have a second cam slot. The cam pin, with a longitudinal axis, can be moveably secured within the first cam slot and the second cam slot. A diameter of the cam pin can be less than a width between a first longitudinal edge that defines a first side of each of the first cam slot and the second cam slot and a second longitudinal edge that defines a second opposing side of each of the first cam slot and the second cam slot so that the cam pin is moveably received by both the first cam slot and the second cam slot. With the first jaw pivoted to at least a first position, the cam pin and first flange can be configured such that the first longitudinal edge is contacted by the cam pin but the second longitudinal edge is spaced from the cam pin. The cam pin and second flange can be configured such that the first longitudinal edge is spaced from the cam pin but the second longitudinal edge is contacted by the cam pin.

An electrode assembly for an electrosurgical instrument includes a housing having an active electrical connector and a return electrical connector configured to operably engage a distal end of an electrosurgical instrument shaft, the housing encapsulating an elongated return electrode and a pair of insulative tubes configured to house a wire-like active electrode. The elongated return electrode includes a clevis at a distal end thereof and operably engages to the return electrical connector at a proximal end thereof. The wire-like active electrode operably engages at one end to the active electrical connector. A donut-like insulator is operably engaged to the clevis of the elongated return electrode and is configured to support the wire-like active electrode therearound. A tensioning mechanism is configured to operably engage an opposite end of the wire-like electrode and tension the wire-like active electrode about the donut-like insulator during assembly.

An electrode unit includes: an electrode supporting member provided with a pair of distal end rigid members, surfaces of which are covered by an electrically insulating material, and an elastic region having lower bending rigidity than bending rigidity of each of the pair of distal end rigid members; an electrode configured with electrode bodies respectively protruding downward from the pair of distal end rigid members of the electrode supporting member and a spanning portion that spans between respective lower end portions of the electrode bodies; and an operation member provided in a proximal end rigid member, and configured to move relative to the proximal end rigid member to cause the electrode to move in a direction in which the electrode protrudes relative to the distal end rigid members.

An electrode unit configured to resect or coagulate tissue inside a subject by using a high-frequency current, including: an electrode supporting portion provided with a pair of distal end rigid portions surfaces of which are covered by an electrically insulating material, and an elastic region portion having lower bending rigidity than bending rigidity of each of the pair of distal end rigid portions, the elastic region portion being provided on a proximal end side of each of the pair of distal end rigid portions; and an electrode configured with electrode bodies respectively protruding downward from the pair of distal end rigid portions and an installation portion that installs respective lower ends of the electrode bodies.

A surgical instrument includes a movable handle movable relative a housing to manipulate an end effector assembly, and a rotation assembly. The rotation assembly includes first and second bodies, where one of the bodies is fixedly disposed within a housing and the other body is rotatably disposed within the housing and fixedly disposed about a shaft. An inner contact ring is fixedly disposed on the first body and includes a first electrical connector. An outer contact ring is fixedly disposed on the first body and includes a second electrical connector. First and second spring contacts maintain electrical contact with the inner and outer contact rings. Each of the first and second spring contacts include a substructure that includes a brush holder, an extension, an electrical connector, and a spring that biases the brush towards the inner or outer contact ring to maintain electrical contact.

A medical device includes an elongated sleeve having a longitudinal axis, a proximal end and a distal end. A cutting member having a plurality of sharp edges is formed from a wear-resistant ceramic material is carried at the distal end of the elongated sleeve. A motor drive is coupled to the proximal end of the elongated sleeve to rotate the sleeve at cutting member at high RPMs to cut bone and other hard tissue. An electrode is carried in a distal portion of ceramic cutting member for RF ablation of tissue when the sleeve and cutting member are is a stationary position. In methods of use, (i) the ceramic member can be engaged against bone and then rotated at high speed to cut bone tissue, and (ii) the ceramic member can be held in a stationary (non-rotating) position to engage tissue and RF energy can be delivered to the electrode to create a plasma that ablates tissue.