
Progressive Surgical Products, Inc.
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PROXIDERM, MODELS TN 460, TN 90 460, BK 460 is an FDA 510(k)-cleared medical device (K982439) manufactured by Progressive Surgical Products, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 7, 1998. Regulation: 8.