Zogenix Inc. have appointed Mallinckrodt to co market Sumavel Dose Pro in the US. The 95-person Zogenix sales force in...
The Trevo Pro Retriever, from Stryker, has been granted 510(k) market clearance by the FDA for clot removal. Approval is...
Medtronic plc announced results from an interim analysis of the first 171 patients (including 71 roll-ins) treated in the OPTIMIZE PRO clinical study The post-market, prospective, multi-center study is evaluating procedural outcomes (including pacemaker rate) associated with procedure-related techniques and post-procedure TAVR (transcatheter aortic valve replacement) care pathways when using the self-expanding, supra-annular Evolut PRO and PRO+ TAVR systems in patients with symptomatic severe aortic stenosis.
The FDA has approved the Absolute Pro Vascular Self-Expanding Stent System, from Abbott, for the treatment of Iliac Artery Disease,...
Biotronik announced it has received FDA approval for its Pro-Kinetic Energy cobalt chromium (CoCr) coronary stent system. The company gained...
MallinckrodtL announced a mutually-agreed upon end of the company�s co-promotion agreement with Zogenix . The co-promotion agreement covered Sumavel DosePro...
Abbott announced that the FDA has approved the company's FreeStyle Libre Pro system, a revolutionary continuous glucose monitoring (CGM) system...
Royal Philips announced FDA 510k-clearance of real-time 3D intracardiac echocardiography (ICE) VeriSight Pro catheter which has the potential to improve standard of care for structural heart disease and electrophysiology procedures.
HeartStitch has received its CE Mark in the European Union for its CoAp Pro device for treatment of mitral valve...
An investigator-initiated study (Pro-FEIBA) evaluated the prophylactic use of FEIBA [Anti-inhibitor Coagulant Complex] from Baxter, to ascertain if it can...