A PZT transducer-horn integrated ultrasonic driving structure consists of a nut, a bolt, a left PZT circular stack, a flange, a right PZT truncated stack and a horn. The horn, the right PZT truncated stack, the flange and the left PZT circular stack are arranged in sequence and connected via the bolt and then fastened via the nut; the right PZT transducer is a truncated cone-shaped stack formed by PZT circular plates; and the right PZT transducer and the horn are integrated to form the ultrasonic driving structure. Considering the dimension of PZT on two sides of the flange and the horn meet the requirements for ultrasonic vibration node and antinode, the dimension of round contour of the circular PZT stack and flange is reduced to increase the thickness of the truncated PZT stack and flange. With the integrated structure, the effect of reducing the contour dimension of the ultrasonic driving surgical device can be obtained, and the outer diameter is reduced to the range of 8-10 mm as compared with the range of 12-15 mm in the prior art, thereby further meeting the application requirements.

An elongate endovascular element for crossing through an obstruction in a blood vessel comprises: a proximal section; a distal tip section of smaller diameter than the proximal section; and a distally-tapering intermediate section extending between the proximal and distal tip sections; wherein the tapered intermediate section has a length that is substantially λ/2 or a multiple of λ/2 , where λ is a wavelength of a driving frequency that will produce longitudinal resonance in the element.

An ultrasonic surgical instrument and method of sealing a tissue includes generating a desired burst pressure in the tissue, sealing the tissue, verifying that the tissue is sealed with further application of at least one of the ultrasonic energy and the RF energy. The ultrasonic surgical instrument further includes an end effector having an ultrasonic blade, an RF electrode, and a controller. The controller operatively connects to the ultrasonic blade and the RF electrode and is configured to direct application of ultrasonic and RF energies according to an initial phase, a power phase, and a termination phase for respectively generating a desired burst pressure in the tissue, sealing the tissue, and verifying the sealing of the tissue while inhibiting transection of the tissue.

A method of fabricating an ultrasonic medical device is presented. The method includes machining a surgical tool from a flat metal stock, contacting a face of a first transducer with a first face of the surgical tool, and contacting a face of a second transducer with an opposing face of the surgical tool opposite the first transducer. The first and second transducers are configured to operate in a D31 mode with respect to the longitudinal portion of the surgical tool. Upon activation, the first transducer and the second transducer are configured to induce a standing wave in the surgical tool and the induced standing wave comprises a node at a node location in the surgical tool and an antinode at an antinode location in the surgical tool.

A vibrating body unit includes a vibration generator, a vibration transmitter and first amplitude enlarger. The vibration generator generates ultrasonic vibration whose amplitude has a predetermined correlation with a frequency. The vibration transmitter has a proximal end and a distal end while the vibration generator is attached from a proximal side, and transmits the ultrasonic vibration to a distal side in a longitudinal axis direction. At least one first amplitude enlarger is provided in the vibration transmitter, and enlarges the amplitude of the ultrasonic vibration at a first amplitude enlargement rate in a direction of transmission of the ultrasonic vibration, the first amplitude enlargement rate having a correlation with the frequency opposite to the predetermined correlation.

A treatment assembly includes: a probe which includes a treatment section at a distal end portion thereof; an inner tube which includes a distal end and into which the probe is inserted in a state that the treatment section of the probe protrudes toward a distal end side with respect to the distal end; an opening which is provided in a side surface of the inner tube and which allows an inner side of the inner tube to communicate with an outer side of the inner tube; a support section which is arranged on the inner side of the inner tube from the outer side of the inner tube through the opening and which is configured to support the probe with respect to the inner tube; and an outer tube which covers the outer side of the inner tube and which is configured to fix the support section.

A treatment device includes a probe having a treatment portion to treat a biological tissue by using the ultrasonic vibration generated in an ultrasonic transducer; an action portion being able to be close to and away from the treatment portion and including a pressing portion that presses the biological tissue to the treatment portion; and a vibration damping portion disposed in a part of the pressing portion in a state of facing the treatment portion, moving following the treatment portion to which the ultrasonic vibration is transmitted when abutting on the treatment portion in a state where the ultrasonic vibration is transmitted to the treatment portion, and prevented from being grinded by the treatment portion to which the ultrasonic vibration is transmitted.

A treatment instrument includes a probe including a treatment portion which treats a treatment target part by ultrasonic vibration, and a back portion provided on a side opposite to the treatment portion. The treatment instrument includes a hollow sheath which surrounds the probe, the sheath having a cutout made to expose the treatment portion. The treatment instrument includes protrusion which is provided in the sheath to cover the back portion on a side opposite to the cutout and which has dimensions smaller than the dimensions of the probe in a direction that intersects with a central axis of the probe.

A method of balancing an ultrasonic instrument having an ultrasonically actuated blade is disclosed. The blade includes a body portion and a step portion extending from the body portion. The body portion comprises a first side, a second side, and a width defined between the first and second sides. The step portion includes a first surface, a second surface, and a cutting edge situated intermediate the first and second surfaces. The second surface extends between a first plane including the cutting edge and a second plane which is parallel to the first plane. The first and second surfaces are not parallel and are oriented such that there is an angle defined therebetween. The method comprises the steps of configuring at least a portion of the blade such that a relationship is substantially equal to zero.

A surgical instrument has an ultrasonic blade that connects to a distal end of an ultrasonic waveguide. A clamp arm assembly is moveable from an opened position for receiving a tissue, toward a closed position for clamping the tissue. A clamp arm actuator connected to the clamp arm assembly directs the clamp arm assembly from the opened position toward the closed position. An outer sheath surrounds at least a portion of the ultrasonic waveguide. The outer sheath includes a cover removably received against a sheath body, and a sheath securement feature able to detachably couple the cover to the sheath body such that the cover can be detached from the sheath body for accessing the ultrasonic waveguide within the outer sheath.