OrthoGrid Hip AI® 4.0

OrthoGrid Hip AI® 4.0 is an FDA 510(k)-cleared medical device (K260077) manufactured by OrthoGrid Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 28, 2026. Regulation: 8.