
Dentauraum, Inc.
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REMANIUM: 200,CS, 380, AND CD is an FDA 510(k)-cleared medical device (K952865) manufactured by Dentauraum, 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 July 25, 1995. Regulation: 8.