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LVIS Corporation
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250239
NeuroMatch
May 23, 2025
K241390
NeuroMatch
November 26, 2024
K222450
LVIS NeuroMatch
June 9, 2023