
Adler Industries, Inc.
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DERMATEC+PLUS(TM)& AMBIDERM(TM) LATEX EXAM GLOVES is an FDA 510(k)-cleared medical device (K891819) manufactured by Adler Industries, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 8, 1989. Regulation: 8.

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