EyeArt v2.2.0

EyeArt v2.2.0 is an FDA 510(k)-cleared medical device (K223357) manufactured by Eyenuk, 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 June 15, 2023. Regulation: 8.