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Endodent, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K863638
GUTTA PERCHA POINTS
October 30, 1986
K863411
GUTTA PERCHA
October 30, 1986
K830814
POINT, PAPER ENDODONTIC
April 6, 1983