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Candulor USA, 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
K122852
PHYSIOSTAR NFC
December 6, 2012
K101814
DIRECT CROWN NATURAL 1
September 27, 2010