
Nomir Medical Technologies, Inc.
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NOVEON, MODEL LS1100-01-0968 is an FDA 510(k)-cleared medical device (K071815) manufactured by Nomir Medical Technologies, 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 November 27, 2007. Regulation: 8.