FDA Grants 510(k) Clearance to Corindus Vascular Robotics for CorPath System October 7, 2015 The system enables the precise control of coronary guidewires and balloon and stent devices. Read More
Vetera Spine Receives FDA 510(k) Clearance for Cervical Fusion Device October 6, 2015 The device features a proprietary porous surface technology. Read More
Novocure Receives CE Mark for Optune System October 6, 2015 The system is designed to improve tumor treating fields therapy. Read More
Dako Receives FDA Approval for Lung Cancer Assay October 6, 2015 The diagnostic can reveal if a patient with advanced non-small cell lung cancer is likely to respond to new form of treatment. Read More
FDA Approves Boston Scientific’s Synergy Bioabsorbable Polymer October 6, 2015 The device is designed to treat coronary artery disease. Read More
EBR Systems Wins CE Mark for Cardiac Resynchronization Therapy Device October 5, 2015 The technology utilizes a proprietary wireless system. Read More
FDA Approves OB-Tools’ Fetal Heart Rate Monitoring Unit October 1, 2015 The monitor will be integrated into the new TrueLabor maternal fetal monitor. Read More
SpineGuard Receives CE Mark for DSG Threaded Drill October 1, 2015 The technology is used during insertion of screw implants in the spine. Read More
Medtronic Receives Expanded FDA Approval for Verify Evaluation System October 1, 2015 The system can be used for basic evaluations of InterStim benefit. Read More
FDA Clears ArtVentive’s 11 mm Endoluminal Occlusion System September 30, 2015 The device offers immediate and complete vessel occlusion. Read More
UVLrx Therapeutics Receives CE Mark for Intravenous Light Therapy System September 30, 2015 The system eliminates the need to remove blood from the body. Read More
Stentys Receives CE Mark for Self-Apposing Coronary Stent September 29, 2015 In a clinical study, the stent prevented foot amputation in 99 percent of patients treated for critical limb ischemia. Read More