
Celestray Biotech Company, LLC.,
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SpinMedix Absorbable Fibrous Membrane is an FDA 510(k)-cleared medical device (K222220) manufactured by Celestray Biotech Company, LLC.,. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 5, 2023. Regulation: 8.