Aeye Health, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Aeye Health, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Apr 2024. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Aeye Health, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and A. Stein - Regulatory Affairs Consulting , Ltd.. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
2 devices