Global Cardiac Bio Implant Devices Market Forecast, Clinical Trials, M&A
Computational model offers insight into mechanisms of drug-coated balloons.
Biosensors International has announced CE Mark approval for BioMatrix NeoFlex, the latest addition to the BioMatrix family of drug-eluting stents (DES).
CE mark received, and Sequent Medical commences a controlled release of these new models in select neurovascular centers in Europe.
Next-Generation Tryton Side Branch SHORT Stent broadens the treatment options in bifurcations in large vessels with a short main branch landing zone.
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.
Elixir Medical Receives CE Mark Approval for the Fully Bioresorbable DESolve Novolimus Eluting Coronary Scaffold System
DiFusion Technologies’ VESTAKEEP PEEK-Based Xiphos ALIF Gains Interbody Fusion Device Receives FDA 510(k) Approval
Zygafix system allows for fusion and stabilization of the facet joint – also termed the zygapophyseal joint.
Zinc: The Perfect Material for Bioabsorbable Stents?
Southern Spine Offers New Minimally Invasive Option for Spine Surgeons
The First International PEEK Meeting Took Place in Philadelphia, Pa.
Curie-Cancer and Vygon partnership look to develop innovative devices, mainly for use in chemotherapy.
Technical Advancements, Procedure Efficiency Result in the Increased Preference for Dental Implants over Traditional Dental Devices
Visit, through a virtual tour, a world-class medtech contract manufacturing facility.