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Reprobitech Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K172751
iVitri Straw
February 9, 2018
K162640
iVitri EZ
June 30, 2017