Neosoma, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neosoma, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Neosoma Brain Mets, NS-HGlio
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.
FDA 510(k) Regulatory Record - Neosoma, Inc.
2 devices