
Zest Anchors, LLC
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LOCATOR OVERDENTURE IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K120198) 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 June 5, 2012. Regulation: 8.