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Vlm Surgical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K945949
KILEJIAN CIRCUMCISION TEMPLATE [THE DOME]
July 25, 1995
K842912
THE SUTURER
August 15, 1984