Varian Medical Systems Receives FDA 510(k) Clearance of its Nexus DRF Digital X-Ray Imaging System
Teleflex Announces Launch of its Next Generation Vascular Positioning System, the ARROW VPS G4 Device
CE Mark for World's Longest Coronary Drug Eluting Stent
Computational model offers insight into mechanisms of drug-coated balloons.
Adapters Pre-Installed on New Machine Shipments; Realize Higher Productivity through Remote Machine Monitoring
Hexagon Metrology Centralized Location Provides One-Stop Resource for Customer Support Needs
Covidien is the Covidien the first company to receive FDA clearance for a motion-tolerant bedside pulse oximeter.
UL Researchers Design New Medical Alloy with Higher X-Ray Visibility
Biosensors International has announced CE Mark approval for BioMatrix NeoFlex, the latest addition to the BioMatrix family of drug-eluting stents (DES).
Rice University students engineer electricity-generating shoes.
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
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.
The Nexus TKO anti-reflux technology reduces the need for occlusion de-clotting medication.
Approval allows extriCARE NPWT system to be sold in the European Union and other countries that recognize or require this.