Oculus Optikger?te GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Oculus Optikger?te GmbH - FDA 510(k) Cleared Devices
Recent clearances: Pentacam® Cornea OCT, Myopia Master
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.
Regulatory submissions have been managed by Hogan Lovells US LLP and Hogan Lovells.
FDA 510(k) Regulatory Record - Oculus Optikger?te GmbH
2 devices