Rejoint YourKnee Receives CE Mark Approval
REJOINT received CE Mark approval for the YourKnee™ patient-specific 3D-printed total knee replacement....
REJOINT received CE Mark approval for the YourKnee™ patient-specific 3D-printed total knee replacement....
Episurf Medical received approval under the CE Mark for the Episealer® Talus and Talus Osteotomy Guide....
Episurf Medical received an additional patent in China relative to the Episealer® Femoral Twin joint implant design process and expects to...
Medacta was granted FDA 510(k) clearance to market MyShoulder Placement Guides for use with the Medacta Shoulder and associated instrumentation....
Episurf Medical's Episealer® knee implant system continues to deliver excellent results in multiple ongoing clinical trials....
Episurf Medical received an additional U.S. patent, “Implant specific drill bit in surgical kit for cartilage repair.” ...
Shoulder Innovations received FDA 510(k) clearance to market InSet Plus™ augmented glenoids for the InSet™ Total Shoulder....
Smith+Nephew announced a limited launch of the new JOURNEY™ II Unicompartmental Knee....
Stryker issued a Safety Communication related to STAR Total Ankle Replacement Non-Foil Packed Mobile Bearing Components....
NextStep Arthropedix launched The Blade™, a femoral stem component for the iNSitu™ Total Hip system....
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