Global Cardiac Bio Implant Devices Market Forecast, Clinical Trials, M&A
Varian Medical Systems Receives FDA 510(k) Clearance of its Nexus DRF Digital X-Ray Imaging System
CE Mark for World's Longest Coronary Drug Eluting Stent
Computational model offers insight into mechanisms of drug-coated balloons.
Covidien is the Covidien the first company to receive FDA clearance for a motion-tolerant bedside pulse oximeter.
Biosensors International has announced CE Mark approval for BioMatrix NeoFlex, the latest addition to the BioMatrix family of drug-eluting stents (DES).
CE mark received, and Sequent Medical commences a controlled release of these new models in select neurovascular centers in Europe.
Covidien Receives FDA 510(k) Clearance for Nellcor Pulse Oximetry Motion Claims
Next-Generation Tryton Side Branch SHORT Stent broadens the treatment options in bifurcations in large vessels with a short main branch landing zone.
Thoratec officials note receipt of approval from FDA to market the HeartMate II Pocket Controller, the small, smart, safe face of the HeartMate II LVAD System.
Aiding physicians in stent placement, next-generation system provides a real-time 360-degree panoramic view of the arteries in 3D.
Investigational Device Exemption allows start of the SALUS feasibility trial of the Direct Flow Medical Transcatheter aortic heart valve system.
Elixir Medical Receives CE Mark Approval for the Fully Bioresorbable DESolve Novolimus Eluting Coronary Scaffold System
Sorin Group’s Remote Monitoring Solution for Patients with Implanted Cardiac Defibrillators
Next-generation implantable defibrillators feature additional safety features to elevate the standard of care.