Neurofield, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurofield, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Genesis Sleep, NeuroField Analysis Suite, Q21
3
Total
3
Cleared
0
Denied
Neurofield, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bishop, US.
Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurofield, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vision28 as regulatory consultant.
FDA 510(k) Regulatory Record - Neurofield, Inc.
3 devices