Carl Zeiss Vision GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Carl Zeiss Vision GmbH - FDA 510(k) Cleared Devices
Recent clearances: VISUREF 600
1
Total
1
Cleared
0
Denied
Carl Zeiss Vision GmbH has 1 FDA 510(k) cleared medical devices. Based in Aalen, DE.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Carl Zeiss Vision GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Carl Zeiss Vision, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Carl Zeiss Vision GmbH
1 devices