
Tecnol New Jersey Wound Care, Inc.
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TECNOL LAZER(TM) SURGICAL MASK is an FDA 510(k)-cleared medical device (K896193) manufactured by Tecnol New Jersey Wound Care, Inc.. 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 February 26, 1990. Regulation: 8.