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Neurofield, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
3
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K252951Genesis SleepDecember 31, 2025
K240420NeuroField Analysis SuiteSeptember 20, 2024
K221959Q21August 31, 2023