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/ Retmap, Inc.
Retmap, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K253586
RM Electrode (RMH 25-01)
April 1, 2026
K232273
RM Electrode (RMH 23-01)
December 7, 2023