5/25/2013
Global Cardiac Bio Implant Devices Market Forecast, Clinical Trials, M&A
5/25/2013
Varian Medical Systems Receives FDA 510(k) Clearance of its Nexus DRF Digital X-Ray Imaging System
5/24/2013
CE Mark for World's Longest Coronary Drug Eluting Stent
5/24/2013
Computational model offers insight into mechanisms of drug-coated balloons.
5/23/2013
Covidien is the Covidien the first company to receive FDA clearance for a motion-tolerant bedside pulse oximeter.
5/22/2013
Biosensors International has announced CE Mark approval for BioMatrix NeoFlex, the latest addition to the BioMatrix family of drug-eluting stents (DES).
5/22/2013
CE mark received, and Sequent Medical commences a controlled release of these new models in select neurovascular centers in Europe.
5/22/2013
Covidien Receives FDA 510(k) Clearance for Nellcor Pulse Oximetry Motion Claims
5/21/2013
Next-Generation Tryton Side Branch SHORT Stent broadens the treatment options in bifurcations in large vessels with a short main branch landing zone.
5/21/2013
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.
5/20/2013
Aiding physicians in stent placement, next-generation system provides a real-time 360-degree panoramic view of the arteries in 3D.
5/20/2013
Investigational Device Exemption allows start of the SALUS feasibility trial of the Direct Flow Medical Transcatheter aortic heart valve system.
5/18/2013
Elixir Medical Receives CE Mark Approval for the Fully Bioresorbable DESolve Novolimus Eluting Coronary Scaffold System
5/15/2013
Sorin Group’s Remote Monitoring Solution for Patients with Implanted Cardiac Defibrillators
5/14/2013
Next-generation implantable defibrillators feature additional safety features to elevate the standard of care.