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Materna Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K220035
Milli Vaginal Dilator
February 27, 2023
K211959
Milli Vaginal Dilator
December 1, 2021