Angiodynamics, Inc. Venacure Procedure Kit

K102796 is the FDA 510(k) clearance record for ANGIODYNAMICS, INC. VENACURE PROCEDURE KIT, a class II device, cleared for AngioDynamics, Inc. on 2010-12-15 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 1,110 510(k) clearances for Boston Scientific Corporation, from 1988-11-23 to 2026-08-12. As of 2026-09-10, FDA records show 16 recalls naming K102796.