xPORT 304 (miCOR) System Lens Fragmentation System

xPORT 304 (miCOR) System Lens Fragmentation System is an FDA 510(k)-cleared medical device (K200584) manufactured by Carl Zeiss Meditec Cataract Technology, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 30, 2020. Regulation: 8.