
L.D. Caulk Co.
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SEALANT, NEW FILLED is an FDA 510(k)-cleared medical device (K760405) manufactured by L.D. Caulk 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 August 22, 1976. Regulation: 8.