
Zest Anchors, Inc.
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ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL) is an FDA 510(k)-cleared medical device (K934668) manufactured by Zest Anchors, Inc.. 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 21, 1994. Regulation: 8.