Medical Device Manufacturer · US , Greenwood Village , CO

Oculus Private Limited - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Oculus Private Limited has 2 FDA 510(k) cleared medical devices. Based in Greenwood Village, US.

Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Ophthalmic.

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

Oculus Private Limited is one of 5275 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Oculus Private Limited — FDA 510(k) Products and Clearance History

2 devices

1-2 of 2