Neuspera Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuspera Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Neuspera Nuity System, Neuspera Neurostimulation System (NNS)
2
Total
2
Cleared
0
Denied
Neuspera Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.
Last cleared in 2023. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuspera Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neuspera Medical, Inc.
2 devices