SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES

SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES is an FDA 510(k)-cleared medical device (K070975) manufactured by Hu-Friedy Mfg. Co., 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 20, 2007. Regulation: 8.