Systems and methods for tourniquet monitoring and control is provided. A system includes at least one sensor, a housing, a processor, and a user communication module. The at least one sensor is configured to monitor at least one of deployment or operation of the tourniquet. The housing is configured to removably engage the tourniquet to position the at least one sensor to monitor the at least one of deployment or operation of the tourniquet. The processor is configured to receive feedback from the at least one sensor, compare the feedback to at least one of deployment or operation parameters for the tourniquet, and generate a user report. The user communication module is configured to communicate the user report.

A method includes receiving: (i) a position of a target tissue intended to be ablated in an organ of a patient and having a predefined pattern, and (ii) an energy level of an ablation signal intended to be applied to the target tissue. One or more selected ablation electrodes that, when applying the ablation signal, produce together a lesion having a shape that covers the predefined pattern, are selected in a catheter that is inserted into the organ and has an array of ablation electrodes. In response to verifying that: (i) the one or more selected ablation electrodes are positioned on the target tissue, and (ii) a contact force between the one or more selected ablation electrode and the target tissue is larger than a force threshold, the ablation signal is applied to the target tissue using the one or more selected ablation electrodes.

A surgical instrument assembly is disclosed. The surgical instrument assembly comprises a shaft, an articulation region, and an end effector attached to the shaft by way of the articulation region, wherein the end effector is configured to be articulated relative to the shaft. The shaft comprises an outer housing, an inner spine positioned with the outer housing, and a core member positioned within the inner spine. The core member comprises a distal end attached to a component the end effector and a proximal end attached to the proximal housing, wherein the core member comprises a material different than a material of the inner spine, and wherein the core member defines a maximum system stretch of the inner spine.

A robotic imaging system includes a camera configured to one or more images of a target site. The camera may be a stereoscopic camera configured to record a left image and a right image for producing at least one stereoscopic image of the target site. A robotic arm is operatively connected to the camera, the robotic arm being adapted to selectively move the camera relative to the target site. A sensor is configured to detect forces and/or torque imparted by a user for moving the stereoscopic camera and transmit sensor data. A controller is configured to receive the sensor data, the controller having a processor and tangible, non-transitory memory on which instructions are recorded. The controller is adapted to selectively execute an assisted drive mode, which includes determining a movement sequence for the robotic arm based in part on the sensor data and a damping function.

Disclosed is a high frequency treatment handpiece having roller electrodes. The handpiece includes: a handpiece casing part; and a plurality of roller electrode members rotatably positioned on a lower surface of the handpiece casing part and applying a high frequency by being brought into contact with the skin. The handpiece prevents burning when the continuous rubbing of a treated area is performed during a treatment, allows a practitioner to conveniently perform the treatment, and allows a person being treated to comfortably receive the treatment with minimum pain. Ball electrodes and roller electrodes can be selectively used, and a roller fixed mode, which limits the rotation of the roller electrodes, can also be selectively used, and thus various massage effects can be selectively provided in accordance with the condition of a patient's skin, and the effect of the high frequency treatment can be maximized by means of the various massage effects.

Various examples are directed to systems and methods for operating a surgical instrument comprising a firing member translatable proximally and distally along a longitudinal axis between a stroke begin position to a stroke end position distal of the stroke begin position; a knife coupled to the firing member; and a motor coupled to the firing member to translate the firing member between the stroke begin position and the stroke end position. A control circuit may receive a firing signal and begin a firing member stroke by providing an initial motor setting to the motor. The control circuit may maintain the initial motor setting for an open-loop portion of the firing member stroke. The control circuit may receive firing member motion data describing a motion of the firing member during the open-loop portion of the firing member stroke and may select a firing control program based at least in part on the motion of the firing member during the open-loop portion of the firing member stroke.

A system and a method are disclosed for forming an anastomosis between a first layer of tissue and a second layer of tissue of a patient's body. The system includes a first anastomosis device component and a second anastomosis device component configured to interact with the first anastomosis device component. The first anastomosis device component is configured to be delivered to a first lumen inside the patient's body. The second anastomosis device component is configured to be delivered to a second lumen inside the patient's body. The second anastomosis device includes one or more sensors configured to capture sensor data for determining an alignment of the second anastomosis device component relative to the first anastomosis device component, or for characterizing the position or orientation of the second anastomosis device component in three-dimensional space.

A surgical robot system includes a slave unit and a computing unit. The slave unit includes a robotic arm, a surgical instrument, a cannula and a sensing element. The robotic arm drives the surgical instrument to rotate about a remote center of motion (RCM). The cannula is detachably coupled to a terminal of the robotic arm and defines an axis passing through the RCM. The surgical instrument is detachably connected with the terminal of the robotic arm and extends distally through the cannula, and the sensing element is disposed on the cannula and senses an axial deformation of the cannula. The computing unit determines a radial force acting on the terminal of the surgical instrument, from a force on the cannula sensed by the sensing element, according to the principle of torque balance. This surgical robot system has force feedback capabilities and obtains the radial force acting on the terminal of the surgical instrument directly from a measurement with higher accuracy and not requiring any additional component, providing for reduced structural complexity of the surgical instrument.

A method for generating intraoperative surgical guidance during a knee arthroplasty includes: preceding resection of a first bone and a second bone in a knee of a patient, generating a first ligament tension curve for a first ligament in the knee; generating a second ligament tension curve for a second ligament in the knee; storing a first target tension curve for the first ligament based on the first ligament tension curve; and, succeeding resection of the first bone and succeeding placement of a first test implant on the first bone, generating a third ligament tension curve for the first ligament; characterizing a first phase difference between the third ligament tension curve and the first target tension curve; and in response to the first phase difference exceeding a threshold negative phase difference, outputting a first prompt to a surgeon to further resect the first bone proportional to the first phase difference.

A surgical instrument includes an ultrasonic waveguide extending through a body assembly. An ultrasonic blade connects to the ultrasonic waveguide. A clamp arm assembly of the surgical instrument is able to move from an opened position for receiving a tissue toward a closed position for clamping the tissue. The clamp arm assembly includes a clamp body and a clamp pad facing the ultrasonic blade. A clamp arm actuator of the surgical instrument is able to move from a first position toward a second position to direct the clamp arm assembly from the opened position toward the closed position. A modular coupling of the surgical instrument connects to the clamp pad such that at least the clamp pad can be disconnected relative to the ultrasonic blade for replacement thereof.