
Bio-Interfaces, Inc.
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4060 POROUS HA PARTICULES BII PORE is an FDA 510(k)-cleared medical device (K924286) manufactured by Bio-Interfaces, 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 April 13, 1993. Regulation: 8.