Neosoma, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Neosoma, Inc. has 2 FDA 510(k) cleared medical devices. Based in Groton, US.
Latest FDA clearance: Dec 2025. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Neosoma, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Innolitics, LLC as regulatory consultant.
2 devices