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Dentatus USA , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K042931
TUF LINK SILICONE RELINER
December 8, 2004
K031793
DENTATUS OSCIOMAT
November 13, 2003
K980620
DENTATUS MTI MODULAR TRANSITIONAL IMPLANTS AND PROSTHETIC SYSTEM
May 15, 1998
K961704
MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM
July 26, 1996