FLEXOR (DENTURE ACRYLIC RELINE MATERIAL)

FLEXOR (DENTURE ACRYLIC RELINE MATERIAL) is an FDA 510(k)-cleared medical device (K902972) manufactured by Cmp Industries, LLC. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 1990. Regulation: 8.