A balloon catheter and methods for use are disclosed for endovascular procedures, e.g., performing a thrombectomy. In one embodiment, among others, the balloon catheter includes an elongated catheter body. At a distal end, the catheter body also includes an angled tip and a balloon adjacent to the angled tip. The balloon is inflatable to form an oblong shape.

A balloon catheter includes a hollow shaft, and an expandable and contractable balloon that covers at least a part of an outer periphery of the hollow shaft. The balloon has a first joint joined to the outer periphery of the hollow shaft, a second joint on a proximal end side with respect to the first joint and joined to the outer periphery of the hollow shaft, and an expandable section continuous with the first joint and the second joint. The first joint is wholly located inside the expandable section. A distal end of the first joint part is spaced apart from a distal end of the hollow shaft toward a proximal end side.

A balloon catheter includes an inflatable balloon disposed on a tip-end side of the balloon catheter. A linear part of an outer surface of the inflatable balloon extends linearly in an axial direction of the inflatable balloon, the linear part has a notch at an intermediate position in a length direction of the linear part, and the notch opens in a direction intersecting the length direction.

A catheter (1) resector balloon (8) used in the treatment of any type of endoluminal-endobronchial tumoral or non-tumoral narrowing and occlusions and endovascular obstructions seen in the hollow tubular organs such as the trachea, esophagus, urinary tract, biliary tract, etc. and vessels, characterized in that, it comprises the following; at least one flexible pad section with pressure and proximity sensor and/or pad section without pressure and proximity sensor which provides soft stopping at the final wall section where the catheter (1) resector balloon (8) is applied in a soft, flexible and shock absorber manner at the tip (2) portion, prevents punctures, tears, bursts or vascular damages occurred in the tissues and vessels formed as a region, undesired complications, provides stopping without giving any damage to its location.

A cage can be positioned around a medical balloon, such as an angioplasty balloon, to assist in a medical procedure. The cage can include a plurality of strips, each extending between a set of rings including first and second rings. As the balloon expands, the first and second rings move closer together and allow the strips to expand outward. The cage may have wedge dissectors on the strips.

A cage can be positioned around a medical balloon, such as an angioplasty balloon, to assist in a medical procedure. The cage can include a plurality of strips, each extending between a set of rings including first and second rings. As the balloon expands, the first and second rings move closer together and allow the strips to expand outward. The cage may have wedge dissectors on the strips.

The disclosed technology includes a balloon guide catheter having a substantially tubular body, an inflation lumen, and a balloon. The tubular body can include an inner hollow lumen and a distal end. The inflation lumen can have a distal end and a proximal section. The distal end of the inflation lumen can be in connection with the tubular body approximate to the distal end of the tubular body. The proximal section of the inflation lumen can extend a majority of the length of the tubular body and can be moveable in relation to the tubular body. The inflation lumen can be positioned within an inner hollow lumen of a tubular body of the catheter or external to the tubular body, thereby enhancing flexibility of the catheter.

Retrieval of material from vessel lumens can be improved by electrically enhancing attachment of the material to the thrombectomy system. The system can include a catheter having a distal portion configured to be positioned adjacent to a thrombus in a blood vessel, an electrode disposed at the distal portion of the catheter, and an interventional element configured to be delivered through a lumen of the catheter. The electrode and the interventional element are each configured to be electrically coupled to an extracorporeal power supply.

A device and method for intravascular treatment of atherosclerotic plaque prior to balloon angioplasty which microperforates the plaque with small sharp spikes acting as serrations for forming cleavage lines or planes in the plaque. The spikes may also be used to transport medication into the plaque. The plaque preparation treatment enables subsequent angioplasty to be performed at low balloon pressures of about 4 atmospheres or less, reduces dissections, and avoids injury to the arterial wall. The subsequent angioplasty may be performed with a drug-eluting balloon (DEB) or drug-coated balloon (DCB). The pre-angioplasty perforation procedure enables more drug to be absorbed during DEB or DCB angioplasty, and makes the need for a stent less likely. Alternatively, any local incidence of plaque dissection after balloon angioplasty may be treated by applying a thin, ring-shaped tack at the dissection site only, rather than applying a stent over the overall plaque site.

Systems, devices and methods for treating a stenosed vessel or heart valve are disclosed. In some embodiments, a cutting/scoring assembly/device for treating a stenosed vessel/heart valve is provided and includes a main, elongated scoring sleeve or element with multiple longitude wires arranged at a distal end. A distal end of the elongated element is proximal to the multiple longitude wires which, when used in conjunction with a balloon catheter, is used to for, according to some embodiments, localized controlled longitudinal vessel incision.