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Neurent Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K261833
NEUROMARK System (NMK00301)
June 16, 2026
K250048
NEUROMARK System (NMK00301)
May 29, 2025
K222032
NEUROMARK System
October 26, 2022
K212666
Neuromark System
October 22, 2021