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Neuroone Medical Technologies Corp.

FDA Regulatory Profile

Neuroone Medical Technologies Corp. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 15, 2025.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251243OneRF Trigeminal Nerve Radiofrequency ProbesAugust 15, 2025
K231675OneRF Ablation SystemDecember 6, 2023
K222404Evo® sEEG SystemOctober 20, 2022
K211367Evo sEEG SystemSeptember 1, 2021

FDA data resources