Quartz Rods Titanium Rods

K862472 is the FDA 510(k) clearance record for QUARTZ RODS TITANIUM RODS, a class II device, cleared for Quali-Med, Inc. on 1986-09-12 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 7 510(k) clearances for Quali-Med, Inc., from 1986-05-16 to 1987-04-27. As of 2026-09-10, FDA records show no recalls naming K862472.