Embolization, Inc. announced findings from the limited-market release of the company’s nitinol enhanced device (NED), which ...

Endospan, an Israel-based developer of solutions for the endovascular repair of aortic arch disease, announced that the FDA ...

Baylis Medical Technologies Inc. announced FDA 510(k) clearance and the commercial launch of the company’s PowerWire 14 radi ...

HistoSonics announced the successful treatments of the first patients in WOLVERINE, a prospective feasibility trial of the ...

Shape Memory Medical has announced the first patient enrollments in the FLAGSHIP study, a prospective single-arm open-la ...

Ellipsys Medical, Inc. announced that the Ellipsys vascular access system will re-enter the market, with commercial availabil ...

Fluidx Medical Technology, Inc. announced that the first patient has been treated with the company’s Ultra embolic gel in a ...

Concept Medical Inc. announced the presentation of primary results of the SirPAD randomized controlled trial of the company’ ...

Serenity Medical announced that the United States FDA has granted Humanitarian Device Exemption (HDE) approval for the River stent ...

Getinge announced it has received FDA premarket approval for additional sizes of its iCast covered stent system. The approval ...

Medtronic announced it is supporting the investigator-initiated EMBRACE trial of the company’s Symplicity Spyral renal dene ...

MicroPort NeuroScientific Corporation announced that the company’s Apollo Dream sirolimus target-eluting stent system has b ...