Please provide your email address to receive an email when new articles are posted on . “SPIRARE opens the door for a new generation of large-bore interventional technology, designed for increased ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. The FDA has identified the recall of LeMaitre Vascular’s ...

MENLO PARK, Calif.--(BUSINESS WIRE)--Jupiter Endovascular, Inc., a medical technology startup developing a new class of endovascular procedures using Endoportal Control™, announced today that the ...

Late-breaking data from the ENGULF trial showed that a novel dual-action thrombectomy device was effective and safe in treating acute pulmonary embolism (PE). The safety and effectiveness results were ...

A pulmonary embolism (PE) is when a pulmonary artery is obstructed by an embolus (usually a blood clot) that travels to the lungs from deep veins in the leg or pelvis. PE often causes shortness of ...

Routine use of the Fogarty embolectomy catheter after cardiac catheterization through a brachial arteriotomy in 25 patients was associated with a decline in major and minor complications from 28 to 4 ...

Long Beach, Calif. – May 3, 2024 – Late-breaking data from the ENGULF trial showed that a novel dual-action thrombectomy device was effective and safe in treating acute pulmonary embolism (PE). The ...

Applied Medical is recalling 19,400 of their Python embolectomy catheters, Bard embolectomy catheters, and OTW Latis cleaning catheters because the catheter tip could detach during use. If this ...

ONE hundred and ninety saddle emboli at the aortic bifurcation have been reported to date. To these we are adding 3 cases, making a total of 193. Two of our 3 patients were treated by embolectomy, and ...

Mechanical embolectomy performed with general instead of local anesthesia is associated with worse clinical outcomes and poorer survival, according to an article published online March 25, 2014, ahead ...