The FDA announced 510(k) clearance for Inari Medical’s FlowTriever device for the treatment of pulmonary embolism (“PE”). According to Inari, the FlowTriever system is the first thrombectomy device ...

A novel thrombectomy, or ‘stent on a wire,’ device continues to show positive results in acute stroke patients, achieving high rates of complete revascularization and good outcomes, especially in ...

The acquisition expands Endologix’s device options for clinical partners already utilising its Detour, Alto, and AFX2 platforms.

Surmodics, Inc. SRDX recently announced the successful early clinical use of the company’s Pounce LP (Low Profile) Thrombectomy System. With the addition of a low-profile device, the Surmodics Pounce ...

Endologix has acquired Surmodics' Pounce System, a platform for non-surgical peripheral arterial thrombi removal, expanding ...

Endologix announced the acquisition of the Pounce thrombectomy system from Surmodics, expanding the company’s portfolio of pe ...

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 ...

Penumbra ($PEN), one of the top devicemaker IPOs last year, unveiled its latest thrombectomy product to the U.S. market. Dubbed the ACE 68 Reperfusion Catheter, the ...

The mechanical thrombectomy devices market is expected to grow at a steady rate during the forecast period. These devices are the gold standard for the treatment of blood clot and revascularization, ...

In essence, all of these devices are used to decrease the time taken for thrombus removal and possibly to reduce the risk of prolonged infusion (Box 1). Percutaneous mechanical thrombectomy (PMT) ...

YOKNEAM, Israel & MIAMI--(BUSINESS WIRE)--Rapid Medical, a leading developer of advanced neurovascular devices, today announced FDA investigational device exemption (IDE) approval for the first-ever ...