
Zest Anchors, LLC
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SATURNO(TM) OVERDENTURE IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K133327) 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 24, 2014. Regulation: 8.