Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Neurofield, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2025-12-31
TypeNumberDevice NameCodeDateActions
510(k) K252951 Genesis SleepQJQ2025-12-31 View
510(k) K240420 NeuroField Analysis SuiteOLU2024-09-20 View
510(k) K221959 Q21GWQ2023-08-31 View