Press Releases
Shape Memory Medical Inc. announced today it has received CE mark for its TrelliX® Embolic Coil System. The TrelliX Embolic Coil System is intended to obstruct or occlude blood flow in vascular
Read more...Ortho Clinical Diagnostics, a global leader of in vitro diagnostics, today announced that ORTHO™ Sera, a suite of extended antigen phenotyping, has been cleared by the U.S. Food and Drug Admi
Read more...18 October 2019
The CE certified products/brands are as listed below: MagicTouch – PTA (Sirolimus Coated PTA Balloon Catheter) for peripheral arterial disease MagicTouch – ED (Sirolimu
Read more...17 October 2019
Molina Healthcare, Inc. announced that it has entered into a definitive agreement to acquire certain assets of YourCare Health Plan, Inc., a not-for-profit subsidiary of Monroe Plan for Medical Car
Read more...16 October 2019
Tactical Medical Solutions, LLC (“TacMed”), a leading innovator and manufacturer of proprietary pre-hospital medical components and technology for tactical and civilian applications, an
Read more...15 October 2019
Hyperfine Research Inc. announced today its collaboration with the Yale School of Medicine to pioneer the use of the world’s first portable, low-cost magnetic resonance imaging (MRI) system a
Read more...14 October 2019
The absolute revolution of nuclear medicine with the emergence of theranostics is forcing all stakeholders involved in the process to come up with new, outside-the-box thinking. Reducing exposure,
Read more...11 October 2019
THINK Surgical, Inc. is pleased to announce it has obtained clearance from the U.S. Food and Drug Administration (FDA) to market the TSolution One® Total Knee Application for use in total knee
Read more...10 October 2019
Medtronic plc today announced it has received Breakthrough Device designation from the U.S. Food and Drug Administration (FDA) for its Valiant® TAAA Stent Graft System for minimally invasive re
Read more...9 October 2019
PQ Bypass, Inc., a clinical-stage medical device company, today announced it has received full approval of its investigational device exemption (IDE) trial of the company’s TORUS stent graft,
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