Aeye Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Aeye Health, Inc.
2 devices