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Dentec, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K894930
DENTEC 4000
March 27, 1990
K864376
FIBERBOND
April 7, 1987
K833429
PERI MIRROR/SALIVA EJECTOR
December 22, 1983