Permatage Flowable, Settable Bone Paste

Permatage Flowable, Settable Bone Paste is an FDA 510(k)-cleared medical device (K253732) manufactured by Orthocon, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 2026. Regulation: 8.