A lithotripsy device can comprise a handpiece, a lithotripsy probe extending from the handpiece, an energization source configured to deliver an energy to a distal end of the lithotripsy probe, a suction passage extending from the distal end of the probe and through the handpiece, and a capture device comprising a container comprising a storage space, an entry port configured to couple to the handpiece at the suction passage, and an exit port, and a capture element connected to the container and configured to facilitate capture of stone fragments within the storage space. A method can comprise fragmenting stones with a lithotripsy device, drawing a vacuum through the lithotripsy device to pull stone fragments and waste fluid therethrough, pulling the vacuum through a stone capture device connected to the lithotripsy device, depositing stone fragments within the stone capture device using a capture element, and drawing the vacuum through the device.

The disclosure relates to a lithotripsy device comprising an elongate probe, which can be inserted into a body interior of a human or animal body, and a drive arrangement for deflecting the probe, which is arranged at a proximal portion of the probe, the drive arrangement comprising an ultrasonic converter unit for exciting ultrasonic vibrations in the direction of a longitudinal extension of the probe, and the drive arrangement having a deflection device for exerting a time-varying force onto the probe in a direction transversely to the longitudinal extension of the probe. The disclosure also relates to a lithotripsy system and to a method for operating a lithotripsy device.

A system to deliver energy to treat a mobile calculus, the system can include a drill and a lateral energy emitter. The drill can be configured to drill a recess into the mobile calculus or a passage through the mobile calculus. The lateral energy emitter can be configured to be advanced into the recess or the passage and to transmit the energy internal to the mobile calculus to fragment the mobile calculus. In some examples, the system can include a deployable capture portion to constrain a stone relative to the capture portion.

An occlusion clearing device for a patient has a housing with a motor(s) that generates repetitive motion, which is reciprocating, rotational or both. A clearing stem including a sheath that has a lumen, wherein aspiration is conducted through the sheath lumen. A wire is located in the sheath lumen and receives repetitive motion from the controller. The sheath terminates in a sheath end having at least one sheath opening. The wire terminates in a wire tip, which may be flat, helical, or tubular. The wire tip is positioned within the sheath end, in proximity to the sheath opening(s), and movement of the wire tip and/or sheath end relative to each other creates shearing forces that break up an adjacent occlusion.

A method for using an endoluminal device to modify an intravascular lesion includes providing an ultrasound-producing mechanism that converts an electric current into vibrational energy at an ultrasonic frequency; providing a sheath including a sheath lumen, wherein the sheath is configured to retract from a first, fully extended position of the sheath and extend from a second, fully retracted position of the sheath; providing a core wire disposed within the sheath lumen of the sheath, the core wire being coupled to the ultrasound-producing mechanism via a sonic connector, the core wire being excited by the vibrational energy at the ultrasonic frequency when the ultrasound-producing mechanism is activated; and retracting the sheath relative to the core wire to expose a working length of a distal portion of the core wire for ultrasound-based modification of one or more intravascular lesions.

A system for aspirating thrombus and delivering an agent includes an aspiration catheter having a supply lumen having a proximal end, a distal end, and a wall, and an aspiration lumen having a proximal end, an open distal end, and an interior wall surface adjacent the open distal end, and at least one orifice at or adjacent the distal end of the supply lumen, in fluid communication with the aspiration lumen and located proximally of the open distal end of the aspiration lumen, wherein the at least one orifice is configured to create a spray pattern that is caused to impinge on the interior wall surface of the aspiration lumen such that the spray pattern upon impinging on the interior wall surface is caused to transform into at least a substantially distally-oriented flow capable of exiting the open distal end of the aspiration lumen.

A system and method for ultrasound treatment is presented. The system and method alternatingly provide microbubbles in a target region containing a biomineralization, then insonate the microbubbles using an external ultrasound source. The microbubbles cavitate in the target region, destructively affecting the biomineralization and potentially breaking it or reducing its mass over time as a result of the cavitation action. Spatial orientation or alignment of the external ultrasound source may be achieved for best results using acoustic signatures and spectral representations of the same.

An ultrasonic catheter system includes an ultrasonic transducer configured to deliver ultrasonic vibrational energy when activated. An ultrasonic catheter is coupled to the ultrasonic transducer to receive the ultrasonic vibrational energy. The ultrasonic catheter includes an elongate flexible catheter sheath and a distal end portion having a longitudinal axis. The distal end portion includes a longitudinal pressure sensor and a distal tip element. The longitudinal pressure sensor is configured to generate a catheter longitudinal pressure signal corresponding to a sensed longitudinal pressure encountered by the ultrasonic catheter along the longitudinal axis of the distal end portion.

An intraluminal scoring system for expanding an opening within an intraluminal passage includes a balloon catheter which is positioned alongside plaque lining a wall of the intraluminal passage. A wire is positioned between the balloon and the plaque so that the inflation of the balloon restricts the wire between the balloon and the plaque. After the balloon is inflated, a mechanical vibration is induced in the proximal end of the wire by a lithotripter actuator. The vibration travels through the wire to the distal portion, causing the wire to impact the plaque lining the wall of the passage causing scoring, compression, or fragmentation of the plaque.

There is described a method of treating a lesion including inserting a waveguide into a vessel of a subject, with a lesion being present in the vessel and the waveguide extending longitudinally between a proximal end and a distal end; positioning the distal end of the waveguide adjacent to the lesion; generating a high amplitude mechanical pulse and propagating the high amplitude pulse from the proximal end to the distal end of the waveguide; and propagating at least a portion of the high amplitude pulse from the distal end of the waveguide to the lesion, the at least one portion of the high amplitude pulse propagating up to the lesion, thereby treating at least partially the lesion.