Medical Device Manufacturer · US , Woodinville , WA

Oculus Optikgerate GmbH - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2003

Total

Cleared

Denied

Oculus Optikgerate GmbH has 6 FDA 510(k) cleared medical devices. Based in Woodinville, US.

Historical record: 6 cleared submissions from 2003 to 2020. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Oculus Optikgerate GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Oculus Optikgerate GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Oculus Optikgerate GmbH

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: May 28, 2026