An intracorporeal pressure shock wave includes an expandable pressure shock wave reflector at the distal end of an intracorporeal catheter to direct shock waves from a shock wave generator within a human or animal blood vessel or body lumen.

A catheter for thromboembolic disease with mechanic waves, injection, and ejection having a triple-lumen catheter system, whereby a first lumen is for injection, a second lumen is for ejection, and a third lumen has a mechanical wave emitter for wave emissions. The first lumen, the second lumen, and the third lumen are longitudinal, whereby the first lumen and the second lumen are symmetrical and opposite each other, and the third lumen is positioned approximately at a center of the triple lumen catheter system.

A dilation balloon is wrapped in one or more patterns with a wire or braided material having diamond abrasive or other abrasive material bonded thereto. The wire or braided material is vibrated in one or more ways to enhance the cutting action of the wire abrasive. The wire abrasive may be vibrated using high, low, or even ultrasonic waves transmitted to the wire abrasive via local or remote methods. Alternatively, the dilation balloon may be dilated with a contrast media that exhibits a high absorption to laser light. The contrast material is lazed with a laser fiber or fibers inserted into the balloon interior, creating a substantial shockwave that vibrates the balloon and assists in the cracking or abrading of the surrounding plaque in contact with the dilation balloon. The cutting balloon may employ the abrasive coated wires described above or cutting blades.

Methods, devices and systems are described for treating venous insufficiency in which the vein is compressed at least partially along a treatment zone. A system can be provided including an injection device, such as a glue gun, that is operably connected to a delivery catheter that can be advanced across a treatment zone in the vein. The delivery catheter can be used to deliver one, two, or more boluses of media (e.g., cyanoacrylate) to occlude the vein along different spaced-apart sections of the treatment zone. External compression can also be applied to the vein by a compression element, such as a hand or multifunctional ultrasound transducer, to occlude portions of the vein along the treatment zone prior to or during the introduction of the boluses of media.

A surgical apparatus for treating a vessel blockage in a vessel of a patient having an elongated member having an outer wall, a first hole at a distal portion and a second hole spaced proximally from the first hole positioned in a side wall. A first lumen is provided within the elongated member for blood flow through the second hole, through the lumen and exiting the first hole to maintain blood flow during treatment of the vessel blockage. A motor driven impeller is rotatable during blood flow through the first lumen to enhance blood flow as blood flows into the second hole positioned proximal of the vessel blockage and exits the first hole distal of the vessel blockage during injection of fluid through one or more openings to treat the vessel blockage.

An ultra-sonic medical dissector includes a vibration generator and a wire that defines a cutting loop remote from a first end and a second end. The wire is coupled to the vibration generator in a cutting configuration, and a cutting surface is located on an inner curvature of the cutting loop. A vibration is generated by the vibration generator is transmitted to the cutting loop by the wire when the wire is in tension. The cutting loop can free an embedded end of a vena cava filter from a vessel wall to ease retrieval.

A vascular occlusion treatment system includes an ultrasound imaging system having an imaging control circuit communicatively coupled to an ultrasound imaging probe and to a display screen, and an ultrasonic vibration system having an ultrasonic generator operatively coupled to a medical ultrasonic object, such as an ultrasonic catheter. The ultrasonic catheter has a corewire with a distal tip. The ultrasonic generator has a generator control circuit that alternatingly switches between an ultrasonic work frequency and a tracking frequency. The generator control circuit sends a notification to the imaging control circuit when the generator control circuit has switched from the ultrasonic work frequency to the tracking frequency. The imaging control circuit responds by initiating a search in an ultrasound imaging space to locate the distal tip that is vibrating at the tracking frequency, and indicating a location of the distal tip in the ultrasound image displayed on the display screen.

An atherectomy device includes a handpiece having an ultrasonic transducer, and an ultrasonic catheter assembly detachably attached to the handpiece. The ultrasonic catheter assembly includes a sheath having a proximal end, a distal end, and an elongate lumen. A core wire is located in the elongate lumen. The core wire has a distal tip and a distal portion proximal to the distal tip. The distal portion has an abrasive exterior surface portion. The abrasive exterior surface portion defines a plurality of cutting protrusions, wherein each of the plurality of cutting protrusions extends away from the core wire in a distal direction at an acute angle with respect to a longitudinal external surface of the core wire.

A surgical apparatus for treating a blood clot in a vessel of a patient having an elongated member having an outer wall, a first hole at a distal portion and a second hole spaced proximally from the first hole positioned in a side wall. A first lumen is provided within the elongated member for blood flow through the second hole, through the lumen and exiting the first hole to maintain blood flow during treatment of the blood clot. An energy emitter emits energy to the blood clot or hardenings and a connector connects the energy emitter to an external energy source, wherein blood flows into the second hole positioned proximal of the blood clot and exits the first hole distal of the blood clot during activation of the energy emitter. In some instances when the apparatus is introduced from a retrograde upstream approach blood may flow through the device in the opposite direction.

An implanted device, such as an inferior vena cava filter, that is partially embedded in soft tissue is retrieved by coupling a vibration device to the implanted device. The implanted device is disembedded from the soft tissue at least in part by generating a vibration with a vibration generator, transmitting the vibration along the vibration transmission apparatus to the implanted device, and vibrating the implanted device. The implanted device is then moved away from the embedding site. A medical device assembly includes the vibration generator, the implantable device and the vibration transmission apparatus.