Oculus Optikger?te GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Oculus Optikger?te GmbH has 2 FDA 510(k) cleared medical devices. Based in Wetzlar, DE.
Latest FDA clearance: Mar 2026. Active since 2021. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculus Optikger?te GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells as regulatory consultant.
2 devices