Disclosed is a method of detecting a short circuit in the jaws of an end effector of a surgical instrument. The method includes applying a sub-therapeutic electrical signal to an electrode located in the jaws of the end effector. The sub-therapeutic electrical signal comprises a sequence of exploratory waveforms comprising pulsed current and voltage waveforms. The method includes detecting a shorted electrode when a measured electrical parameter in the jaws of the end effector is less than a predetermined value and modifying electrical current applied to the shorted electrode by the RF generator.

Disclosed are surgical instruments configured to control therapeutic energy application to tissue based on cartridge and tissue parameters.

A surgical instrument comprising a translatable closing bar and a translatable firing bar is disclosed.

Disclosed is a surgical system for tissue treatment using therapeutic energy and stapling.

A staple cartridge comprising a cartridge body including staple formation features is disclosed.

Apparatus and methods are disclosed for correcting deformities in a patient's foot. In one example, a metatarsus adductus is addressed using a pin placement guide that is angulated to be placed in alignment with a cuneiform and a metatarsal, such that the TMT joint can be subsequently cut, and the metatarsal moved into proper alignment. Th pin placement guide can be a variable angle guide, or a kit of fixed-angle pin placement guides can be provided.

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.

Described are fibula malleolus caps and surgery devices with fibula malleolus caps. The fibula malleolus caps may be patient-specific fibula malleolus caps. The devices with patient-specific fibula malleolus caps overcome the sliding and rotational errors during fibula flap harvesting. A comparative clinical study demonstrates that the fibula malleolus cap enhances the accuracy of fibula flap harvesting, leading to accurate location and angulation of simultaneous dental implants.

Embodiments of the present disclosure include a system for determining an error associated with an electrode disposed on a medical device. The system comprises a processor and a memory storing instructions on a non-transitory computer-readable medium. The instructions are executable by the processor to receive an electrode signal from the electrode disposed on the medical device. The instructions are further executable by the processor to receive a plurality of other electrode signals from a plurality of other electrodes disposed on the medical device. The instructions are further executable by the processor to determine that the electrode signal received from the electrode disposed on the medical device is an outlier in relation to the plurality of other electrode signals from the plurality of other electrodes disposed on the medical device, based on a comparison between the electrode signal and the plurality of other electrode signals.

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.