AltiVate Reverse® ADLC Glenosphere

AltiVate Reverse® ADLC Glenosphere is an FDA 510(k)-cleared medical device (K252567) 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 January 14, 2026. Regulation: 8.