Akesis, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akesis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Akesis Galaxy RTi, Akesis Galaxy RTx, Akesis Galaxy
3
Total
3
Cleared
0
Denied
Akesis, Inc. has 3 FDA 510(k) cleared medical devices. Based in Concord, US.
Last cleared in 2021. Active since 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Akesis, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Akesis, Inc.
3 devices