Fifth Eye, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fifth Eye, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AHI System, AHI System
3
Total
2
Cleared
1
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.
Regulatory submissions have been managed by Biologics Consulting Group and Biologics Consulting.
FDA 510(k) Regulatory Record - Fifth Eye, Inc.
3 devices