
Dexide, Inc.
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DEXIDE DIS. SUR. SCRUB SPONGE W/PARACHLO is an FDA 510(k)-cleared medical device (K792272) manufactured by Dexide, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 26, 1979. Regulation: 8.