ZAROLAN, DUALAN, TITAN AND SUPERON

ZAROLAN, DUALAN, TITAN AND SUPERON is an FDA 510(k)-cleared medical device (K891698) manufactured by Dent Zar, 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 June 8, 1989. Regulation: 8.