MICOR Lens Fragmentation System

MICOR Lens Fragmentation System is an FDA 510(k)-cleared medical device (K214028) 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 September 8, 2022. Regulation: 8.