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.

FDA 510(k) cleared devices by Oculus Optikgerate GmbH

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 6,915 total devices indexed.

Last updated: Apr 27, 2026