VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY

VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY is an FDA 510(k)-cleared medical device (K932893) manufactured by Vident. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 27, 1994. Regulation: 8.