Femtec Laser Microkeratome

K033354 is the FDA 510(k) clearance record for FEMTEC LASER MICROKERATOME, a class II device, cleared for 20/10 Perfect Vision Optische Gerate GmbH on 2004-02-18 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 20/10 Perfect Vision Optische Gerate GmbH. As of 2026-09-10, FDA records show no recalls naming K033354.