Aion Biosystems, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Aion Biosystems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Darien, US.
Latest FDA clearance: Mar 2025. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Aion Biosystems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
2 devices