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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