A method and system for supporting an HF surgical procedure in which tissue is treated. The method includes supplying an HF instrument including an HF electrode and an HF generator with HF current, providing a plurality of HF modes adapted to respective ones of a plurality of tissue types, and orienting an optical capturing device toward the HF electrode such that a field of view of the optical capturing device is configured to encompass a region of the tissue to be treated around the HF electrode during an intended treatment of the tissue. The method further includes performing an optical classification of a tissue type of the tissue in the region of the HF electrode based on optical measurement signals captured by the optical capturing device, and setting a specific HF mode for the tissue type based on the result of the optical classification.

A surgical cautery device includes a voltage generator, a controller, forceps, an actuator, and a receiver. The voltage generator is configured to be electrically connected to a power source. The forceps are electrically coupled to the voltage generator and configured to cauterize tissue. The actuator is configured to generate and wirelessly transmit an on/off signal. The receiver is operable to wirelessly receive the on/off signal. The controller controls power to the voltage generator from the power source in response to the on/off signal.

A dermal conditioning device for creating at feast one fissure, in a stratum corneum layer of an area of skirt, comprising: a non-invasive fissuring generator; a controller coupled to the non-invasive skin fissuring generator, a power supply coupled to the non-invasive skin fissuring generator and the controller; and a housing encasing the non-invasive skin fissuring generator and the controller, wherein the controller controls the non-invasive skin fissuring generator to: generate at least one signal, and apply the at least one signal to dehydrate the area of skin, and stress the external surface of the stratum corneum layer of the area of skin, the stress calibrated to produce a strain on the stratum corneum layer causing a formation of at least one fissure in the stratum corneum layer when the area of skin is dehydrated, while maintaining a pre-fissure immune status of the area of skin.

Described herein is a system including a catheter, an optical circuit, a pulsed field ablation energy source, and a processing device. The catheter includes a proximal section, a distal section, and a shaft coupled between the proximal section and the distal section. The optical circuit is configured to transport light at least partially from the proximal section to the distal section and back. The pulsed field ablation energy source is coupled to the catheter and configured to transmit pulsed electrical signals to a tissue sample. The processing device is configured to analyze one or more optical signals received from the optical circuit to determine changes in polarization or phase retardation of light reflected or scattered by the tissue sample, and determine changes in a birefringence of the tissue sample based on the changes in polarization or phase retardation.

Methods and systems for performing ablation are disclosed. An example system for performing ablation on a tissue includes a catheter having at least one lumen in which a first optical fiber configured to carry a first light beam is disposed and a second optical fiber configured to carry a second light beam is disposed, and a processor being configured to measure a volume of blood within the target site of the tissue using a blood perfusion sensor, determine that the volume of blood within the target site is below a predetermined threshold based on one or more characteristics detected by the blood perfusion sensor, each characteristic being associated with at least one of the first light beam and the second light beam, and perform the ablation on the target site of the tissue when the volume of blood within the target site is below the predetermined threshold.

An instrument for coagulation and dissection of biological tissue including a tool with coagulation electrodes and at least one cutting electrode. The electrodes are actuated via an operating circuit including an evaluation circuit, to which an external apparatus delivers an evaluation signal with first and second half-waves having opposite polarities. During at least one first half-wave, the evaluation circuit checks whether a first switch or a second switch are actuated on the instrument. Depending on the evaluation result, a triggering signal is transmitted to a switching unit. Depending on the triggering signal, the switching unit is switched into a first or second switching state. In the second switching state, no voltage suitable for dissection and no current suitable for dissection, respectively, is applied to the cutting electrode. In the first switching state, a voltage suitable for dissection or a current suitable for dissection is applied to the cutting electrode.

A surgical instrument includes a housing, energizable member, first activation switch, cable assembly, and second activation switch. The housing is operatively associated with the energizable member. The first activation switch is coupled to the energizable member and is selectively transitionable from an open condition to a closed condition. The cable assembly is coupled to the housing at a first end and includes a plug at a second, opposite end, the plug housing a second activation switch selectively transitionable from an open condition to a closed condition. The plug is adapted to connect to the source of electrosurgical energy, wherein transitioning of the first activation switch from the open condition to the closed condition transitions the second activation switch from the open condition to the closed condition such that the second activation switch communicates with the source of electrosurgical energy to initiate the supply of energy to the energizable member.

A surgical instrument includes a housing, energizable member, first activation switch, cable assembly, and second activation switch. The housing is operatively associated with the energizable member. The first activation switch is coupled to the energizable member and is selectively transitionable from an open condition to a closed condition. The cable assembly is coupled to the housing at a first end and includes a plug at a second, opposite end, the plug housing a second activation switch selectively transitionable from an open condition to a closed condition. The plug is adapted to connect to the source of electrosurgical energy, wherein transitioning of the first activation switch from the open condition to the closed condition transitions the second activation switch from the open condition to the closed condition such that the second activation switch communicates with the source of electrosurgical energy to initiate the supply of energy to the energizable member.

A surgical instrument includes a housing, energizable member, first activation switch, cable assembly, and second activation switch. The housing is operatively associated with the energizable member. The first activation switch is coupled to the energizable member and is selectively transitionable from an open condition to a closed condition. The cable assembly is coupled to the housing at a first end and includes a plug at a second, opposite end, the plug housing a second activation switch selectively transitionable from an open condition to a closed condition. The plug is adapted to connect to the source of electrosurgical energy, wherein transitioning of the first activation switch from the open condition to the closed condition transitions the second activation switch from the open condition to the closed condition such that the second activation switch communicates with the source of electrosurgical energy to initiate the supply of energy to the energizable member.

An arthroscopy handpiece includes a handle body and a plurality of electrical components carried by the handle body. The electrical components may be connected to an external controller and power supply remote from the handle body. Typical electrical components include a motor and radiofrequency (RF) contacts adapted for coupling to a disposable electrosurgical tool. The handle body is usually both thermally and electrically conductive, and insulator elements are disposed between the electrical components and the handle body, with each insulator element adapted to prevent a potential leakage current flow from an electrical component to the handle body to prevent accidental electrical shock to the user.