
Remington Products Company, LLC
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REMINGTON TANFASTIC COUNTERTOP FACIAL TANNER is an FDA 510(k)-cleared medical device (K895409) manufactured by Remington Products Company, LLC. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 19, 1989. Regulation: 8.