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Refine USA, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
3
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K192138Rejuvapen NXTApril 9, 2020
K112334VEIN-GOGH INSTRUMENTMay 8, 2012