A debrider that includes an outer tubular member, and an inner tubular member located inside the outer tubular member. The inner tubular member includes an aspiration channel. The outer tubular member includes a declogging feature. The declogging feature extends from an inside distal wall of the outer tubular member in a proximal direction towards a distal wall of the inner member. The declogging feature is at least partially received into the aspiration channel through a distal opening defined in the distal end of the inner member, and is configured to push any matter located inside the aspiration channel in a proximal direction.

A cutting assembly for a surgical instrument. A tube assembly includes an outer tube having an outer cutting window, and an inner tube coaxially disposed within and rotatable relative to the outer tube. The inner tube includes an inner cutting window such that the inner and outer cutting windows define a cutting window of the tube assembly. A portion of the inner tube distal a proximal boundary of the cutting window may define a distal region of the inner tube. A projection is within a lumen of the inner tube with at least a portion of the projection disposed within the distal region. The projection may be an insert. The projection occupies a volume of the distal region and/or reduces a cross-sectional area of the lumen distal to the proximal boundary. The projection reduces the size of material removed through the cutting window to reduce clogging of the tube assembly.

A system for treating a medical condition comprises: a harvesting device for harvesting tissue from a mammalian subject at a harvest site; and a depositing device for depositing material in a patient at a deposit site, the material based on the harvested tissue. The deposited material is configured to generate resultant tissue configured to treat the medical condition of the patient. Methods are also provided for treating a medical condition of a patient.

A surgical instrument (1000) includes an end effector assembly (200) including first and second grasping components (210, 220) each defining a tissue-contacting portion (214, 218, 224, 228). One or both of the first or second grasping components (210, 220) is movable relative to the other between an open position and a closed position. In the closed position, the first and second tissue-contacting portions (214, 218, 224, 228) cooperate to define a grasping area therebetween. One or both of the first or second grasping components (210, 220) is configured to apply energy from the tissue-contacting portion (214, 218, 224, 228) thereof to tissue disposed within the grasping area to treat tissue. The tissue-contacting portion (214, 224) of the first grasping component (210) defines a first opening (219) therethrough. The first opening (219) is disposed within the grasping area and in communication with a first lumen (118) defined at least partially through the first grasping component (210). The first lumen (118) is adapted to connect to a source of vacuum (300) to enable aspiration through the first opening (219).

A method of manufacturing an ultrasound probe includes: forming a probe body; forming a coating portion by applying a liquid containing a resin component as a main component and a filler to a predetermined region on an outer surface of the probe body and heating the liquid; and forming a mold portion by placing the probe body on which the coating portion is formed in a die and pouring a resin containing a same component as the resin component serving as the main component of the coating portion in the die.

A tube configured to be mounted on an outer side of a shaft of a treatment instrument includes a tube main body, and a convex portion that is provided along a longitudinal axis of the tube main body and is protruded inwards in a radial direction of the tube main body with respect to an inner peripheral surface of the tube main body.

A lithotripter is provided for fragmenting a stone inside a patient's body. In one form, the lithotripter includes a motor having at least two modes of operation and is configured to produce first and second waveforms. A wave guide shaft is configured to transmit the first and second waveforms to the stone. In one form, at least one of the first and second waveforms is provided to the stone at a frequency that is about equal to a natural frequency of the stone. In a variation, the lithotripter may include an ultrasonic driver configured to produce an ultrasonic frequency waveform and a sonic driver configured to produce a sonic frequency waveform. The sonic driver is mechanically coupled to the ultrasonic driver. The ultrasonic driver and the sonic driver may be disposed within a driver housing. In another variation, the lithotripter may include a brushless DC motor.

Provided is a medical device for clearing an obstruction from a surgical instrument or surgical site, the device comprising: a first hollow member configured to allow air or inert gas passage; a second hollow member having a distal end and a proximal end, the proximal end configured to be connectable to a vacuum or suction source; a housing member configured to receive both the first hollow member and the second hollow member; and a push button operably connected to the housing member; and an inflation bulb configured to be attachable to the housing member, wherein the push button is configured to disengage the first hollow member and occlude the second hollow member when depressed by a force, and/or wherein the push button and the inflation bulb are configured to be operable by one hand of an operator.

An instrument includes an ultrasonic blade, a first fluid port, an irrigation member, a second fluid port, and a fluid communication assembly. The ultrasonic blade defines a distal opening. The ultrasonic blade is operable in a first mode to emulsify tissue that is distally positioned relative to the ultrasonic blade. The ultrasonic blade is further operable in a second mode to transect and seal tissue that is transversely positioned relative to the ultrasonic blade. The first fluid port is in communication with the distal opening of the ultrasonic blade. The irrigation member is positioned adjacent to the distal end of the ultrasonic blade. The second fluid port is in communication with the irrigation member. The fluid communication assembly is configured to couple the first fluid port with a fluid source, couple the first fluid port with a suction source, and couple the second fluid port with the fluid source.

A surgical device. The surgical device may comprise a transducer configured to provide vibrations along a longitudinal axis and an end effector coupled to the transducer and extending from the transducer along the longitudinal axis. The surgical device also may comprise a lower jaw extending parallel to the end effector. The lower jaw may comprise a clamp face extending toward the longitudinal axis. Also, the lower jaw may be slidable relative to the end effector to bring the clamp face toward a distal end of the end effector.