
Osteogenics Biomedical, Inc.
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Cytoplast Titanium-Reinforced PTFE Membranes is an FDA 510(k)-cleared medical device (K201187) manufactured by Osteogenics 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 January 22, 2021. Regulation: 8.