News

Hansen Medical, Inc., the global leader in flexible robotics and the developer of robotic technology for accurate 3D control of catheter movement, announced that a team of physicians led by Professor Nick Cheshire at St. Mary's Hospital, part of...

Pioneer Surgical Technology, Inc. has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market FortrOss, a novel bone graft substitute utilizing the power of nanotechnology for orthopaedic applications. The FortrOss bone void filler is a...

B. Braun Medical Inc.announced that it had received 510(k) clearance from the FDA for the industry’s first silver-impregnated antibacterial Luer Access Device (LAD) designed to reduce potential catheter-related bloodstream infections.  B. Braun’s ULTRASITE® Ag Luer Access Device uses...

Boston Scientific Corporation announced one-year data from its landmark SYNTAX trial comparing percutaneous coronary intervention (PCI) using the TAXUS® Express2™ Paclitaxel-Eluting Coronary Stent System to contemporary coronary artery bypass graft (CABG) surgery. Boston Scientific Corporation announced one-year data...

BSD Medical Corporation announced that the company has agreed to collaborate with GE Medical Systems in the integration of BSD Medical’s premier cancer treatment system with a GE magnetic resonance imaging (MRI) system. BSD Medical Corporation announced that...

TomoTherapy Incorporated announced that it has received FDA 510(k) clearance for its TomoDirect™ radiation therapy technology. TomoDirect is an innovative new discrete-angle, sliding-beam delivery mode for the Hi·Art® treatment system. With this capability, clinicians gain an efficient complement to...

Alquest, Inc. the leading contract research organization specialized in medical and diagnostic devices – recently helped its client, Biotest Medical Diagnostics GmbH, earn BLA (biologics license application) approvals through the Office of Blood Research and Review in the Center...