
Columbus Dental Mfg. Co.
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LUMIFOR(TM) COMPOSITE is an FDA 510(k)-cleared medical device (K871165) manufactured by Columbus Dental Mfg. 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 April 2, 1987. Regulation: 8.