MODIFICATION TO LINER II: SOFT RELINE LIQUID

MODIFICATION TO LINER II: SOFT RELINE LIQUID is an FDA 510(k)-cleared medical device (K991687) manufactured by Bosworth Co.. 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 6, 1999. Regulation: 8.