Technosanat Kryo Tsk 2005

K992536 is the FDA 510(k) clearance record for TECHNOSANAT KRYO TSK 2005, a class II device, cleared for Technosanat Innovative Medizintechnik GmbH on 1999-10-08 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 Technosanat Innovative Medizintechnik GmbH. As of 2026-09-10, FDA records show no recalls naming K992536.