Medical Device Manufacturer · US , Ann Arbor , MI

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

3 submissions · 2 cleared · Since 2021

Total

Cleared

Denied

Fifth Eye, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.

Last cleared in 2022. Active since 2021. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Fifth Eye, Inc.

3 devices

1-3 of 3