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Aci, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K063753GFX NERVE ABLATION SYSTEMJune 20, 2007
K061501FLEXO DENTAL RESIN MATERIALJuly 26, 2006