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FDA 510(k) Applications Submitted by IVOCLAR USA, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012877
08/27/2001
HIGH GOLD PALLADIUM FREE CERAMIC SOLDER
IVOCLAR USA, INC.
K980986
03/17/1998
PROCAD
IVOCLAR USA, INC.
K981264
04/07/1998
ARISTON PHC
IVOCLAR USA, INC.
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