IMPROVED TRY-IN GEL

IMPROVED TRY-IN GEL is an FDA 510(k)-cleared medical device (K001899) manufactured by Sybron Dental Specialties, 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 August 27, 2000. Regulation: 8.