AltiVate Reverse® Glenoid

AltiVate Reverse® Glenoid is an FDA 510(k)-cleared medical device (K252141) manufactured by Encore Medical L.P.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 2025. Regulation: 8.