Refine USA, LLC

FDA Regulatory Profile

Refine USA, LLC appears in FDA public data with 0 recalls, 2 510(k) clearances, 3 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on Apr 9, 2020.

Summary

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

Recent 510(k) Clearances

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