Vista Ophthalmics Vitrectomy Probe

Vista Ophthalmics Vitrectomy Probe is an FDA 510(k)-cleared medical device (K220030) manufactured by Vista Ophthalmics, LLC. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 3, 2022. Regulation: 8.