LOCATOR® Angled Abutment

LOCATOR® Angled Abutment is an FDA 510(k)-cleared medical device (K252944) manufactured by Zest Anchors, LLC. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 14, 2025. Regulation: 8.