Wave Form Manufacturing Prolase General Shaped Fiber

K020673 is the FDA 510(k) clearance record for WAVE FORM MANUFACTURING PROLASE GENERAL SHAPED FIBER, a class II device, cleared for Wave Form Mfg., Inc. on 2002-05-30 under FDA product code GEX (Powered Laser Surgical Instrument). FDA's definition for product code GEX reads: "A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue...". FDA records list one 510(k) clearance for Wave Form Mfg., Inc. As of 2026-09-10, FDA records show no recalls naming K020673.