
Cosmedent, Inc.
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Renamel® Microhybrid ;Renamel® Flowable Microhybrid is an FDA 510(k)-cleared medical device (K222435) manufactured by Cosmedent, 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 October 10, 2022. Regulation: 8.