Medical Device Manufacturer · US , Carrollton , TX

Raven Eye, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996

Total

Cleared

Denied

Raven Eye, Inc. has 2 FDA 510(k) cleared medical devices. Based in Carrollton, US.

Historical record: 2 cleared submissions from 1996 to 1996. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Raven Eye, Inc. Filter by specialty or product code using the sidebar.

Raven Eye, Inc. 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 - Raven Eye, Inc.

2 devices

1-2 of 2