Ardent Intl., Inc.

FDA Regulatory Profile

Ardent Intl., Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 24, 1986.

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