
Unicare Biomedical, Inc.
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CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090 is an FDA 510(k)-cleared medical device (K090083) manufactured by Unicare Biomedical, 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 March 22, 2009. Regulation: 8.