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Ardent Intl., Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K864300SILIVA EJECTOR/ORAL CAVITY EVACUATORNovember 24, 1986
K842512EXACTA-FILMJune 27, 1984
K832647ARTICULATING PAPERFebruary 21, 1984