Medical methods and devices for treating aortic dissections. A catheter-based cutting device permits cutting a septum of acute or chronic aortic dissections, in a retrograde manner. The catheter includes a base section having a central lumen therethrough and two flexible arms extending from a distal end thereof. The flexible arms can each have a guide wire channel therethrough. With distal ends of the two flexible arms separated, the two arms form a Y-shape with the base section. In one embodiment, with distal ends of the two flexible arms together, the two arms have a longitudinal profile, about a periphery thereof, identical to a longitudinal profile of the base section. A cutting component resides between the two arms. The cutting component can face distally outward between the two arms with the distal ends of the two flexible arms separated.

A treatment instrument includes: a sheath; and an end effector that is provided at a distal end of the sheath. The end effector is capable of gripping a living tissue and applying high frequency energy to the living tissue. The end effector includes a treatment surface, and a pair of electrodes that can grip the living tissue and apply the high frequency energy to the living tissue. The treatment surface includes a distal end area that is provided on a distal end side of the treatment surface, and another area that is provided on a proximal end side of the treatment surface. The distal end area applies, to the living tissue, high frequency energy that is higher than high frequency energy applied by the other area. One of the pair of electrodes includes a distal end portion and a proximal end portion.

An ultrasonic device may include an electromechanical system defined by a resonant frequency and further include an ultrasonic transducer coupled to an ultrasonic blade. The device may be composed of two or more components, one of which is reusable and one of which is disposable. A method of detecting a proper installation of the components may include determining a spectroscopy signature of the blade coupled to the transducer, comparing the signature to a reference signature, determining an installation state of the components based on the comparison, and controlling a delivery of power to the transducer based on the comparison. The method may include enabling an operation of the device when the installation state of components is proper. The method may further include disabling the device when the installation state is not proper and generating a warning. The warning may be visible, audible, or tactile.

A forceps including a gripping assembly. The gripping assembly includes an upper jaw and a lower jaw. The upper jaw includes a proximal end and a distal end. The upper jaw includes an upper tooth having an upper proximally facing canted tooth surface and an upper distally facing canted tooth surface. The lower jaw includes a proximal end and a distal end. The lower jaw includes a socket having a lower distally facing canted socket surface and a lower proximally facing socket surface. The upper jaw, the lower jaw, or both are moveable so that the gripping assembly moves between an open position and a gripping position, in the gripping position, a gap is defined between the upper distally facing canted tooth surface and the lower proximally facing socket surface.

An end effector assembly includes first and second jaw members movable between an open and closed position to grasp tissue therebetween. First and second proximal flanges extending proximally from the second jaw member and defining a space therebetween, a proximal flange extend proximally from a proximal portion of the first jaw member and define a cam slot. A cam driver operably is coupled to the proximal flange of the first jaw member to define a space between the cam driver and the proximal flange of the first jaw member. A cam bar is disposed within the space defined between the cam driver and the proximal flange of the first jaw member. The cam bar includes a cam pin configured to move within a cam slot of the cam driver to move the first jaw member relative to the second jaw member between the open position and the closed position.

In general, surgical devices including visual indicators thereon are provided. A user of the device therefore may quickly visually ascertain various operational details of the surgical device and/or various pieces of information about the device and/or tissue of a patient being operated on.

A vessel sealing device having a pair of electrodes that are maintained in spaced apart configuration when closed by non-uniform coating formed from a non-conductive material that has been applied to roughened electrodes so that the coating allows for the passage of a predetermined amount of radiofrequency (RF) energy between the electrodes. The coating has a predetermined thickness that spaces the electrodes apart while also having the predetermined non-uniformity that allows RF energy to pass between the electrodes when a vessel is trapped therein, thus desiccating the vessel positioned in the jaws. The electrodes may include a series of grooves in a herringbone pattern, with each electrode having the pattern oriented in the same direction or in opposite directions.

A surgical instrument connectable to a surgical energy module that is configured to provide a first drive signal at a first frequency range for driving a first energy modality and a second drive signal at a second frequency range for driving a second energy modality is provided. The surgical instrument can comprise a surgical instrument component configured to receive power from a direct current (DC) power source, an end effector, and a circuit. The circuit can be configured to convert the first electrical signal to a DC voltage, apply the DC voltage to the surgical instrument component, and deliver the second energy modality to the end effector according to the second drive signal. Alternatively, the circuit can be disposed within a cable assembly configured to connect the surgical instrument to the surgical energy module.

A surgical instrument includes a housing having a shaft extending therefrom for supporting an end effector assembly. A handle is disposed on the housing and is selectively moveable relative thereto to actuate the end effector assembly. A PCB is disposed within the housing and includes one or more accelerometers and a timing circuit having a first timer. The accelerometer is configured to activate the first timer of the timing circuit upon detecting movement of the surgical instrument after the surgical instrument is coupled to an electrosurgical energy source. A deactivating assembly is disposed within the housing and is operably associated with the timing circuit such that after expiration of the first timer, the deactivation assembly mechanically decommissions the surgical instrument for continued or subsequent use.

An electrosurgical instrument is provided that captures, compresses, fuses and cuts tissue between upper and lower jaws connected to pivotably movable handles. The instrument includes a force and over compression regulation mechanism that is configured such that in a clamped configuration, the jaws delivers a gripping force between the first jaw and the second jaw between a predetermined minimum force and a predetermined maximum force.