Tenex Receives FDA Clearance for TX2 MicroTip to Treat Chronic Tendinosis
Tenex Health received FDA 510(k) clearance to market the TX2 MicroTip, with application to treat tendinosis of the shoulder and hip...
Tenex Health received FDA 510(k) clearance to market the TX2 MicroTip, with application to treat tendinosis of the shoulder and hip...
Carestream Health filed its FDA 510(k) application for the CARESTREAM OnSight 3D system for weight-bearing extremity imaging....
BioPoly received approval under the CE Mark for the BioPoly® RS Partial Resurfacing Shoulder. ...
On 4/20/16, FDA’s Orthopaedic and Rehabilitation Devices Panel will meet regarding the PMA for Cartiva’s Synthetic Cartilage Implant, an organic polymer-based biomaterial...
Cayenne Medical commenced U.S. launch of the BioWick™ SureLock™ implant, an interpositional scaffold wick designed to address the biology issue associated with...
Proxy Biomedical has developed high strength resorbable USP 2 suture for fracture and soft tissue repair applications. ...
FDA tentatively scheduled a 2Q16 meeting of the Orthopaedic and Rehabilitation Devices Panel to review Cartiva’s Premarket Approval Application for the Synthetic Cartilage Implant in...
Active Implants initiated SUN (Safety Using NUsurface®), a 2nd clinical trial evaluating the investigational meniscus implant....
Episurf Medical achieved a milestone of 100 accounts approved and connected to the company’s proprietary ?ifidelity™ IT platform, used with...
Episurf Medical received CE Mark approval for the Epioscopy™ Damage Assessment Tool, designed to support 3D visualization of knee segments,...
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