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Wave Form Mfg., Inc.
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WAVE FORM MANUFACTURING PROLASE GENERAL SHAPED FIBER is an FDA 510(k)-cleared medical device (K020673) manufactured by Wave Form Mfg., 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 May 29, 2002. Regulation: 8.