
Orthocon, Inc.
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DBX-H HEMOSTATIC DEMINERALIZED BONE MATRIX PUTTY is an FDA 510(k)-cleared medical device (K061131) manufactured by Orthocon, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 7, 2007. Regulation: 8.