ZEPTO Precision Capsulotomy System

ZEPTO Precision Capsulotomy System is an FDA 510(k)-cleared medical device (K210827) manufactured by Centricity Vision, 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 December 13, 2021. Regulation: 8.