
The Kendall Company, L.P.
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KERLIX MD ANTIMICROBIAL GAUZE DRESSING is an FDA 510(k)-cleared medical device (K990530) manufactured by The Kendall Company, L.P.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 30, 2000. Regulation: 8.