K-number	K121359
Device name	IPS 99 ONE AND IPS 99 CERAM
Applicant	Ivoclar Vivadent, AG
Product code	EIH
Device class	Class II
Decision date	Jul 27, 2012
Decision	Substantially Equivalent
Regulation	872.6660

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Source

View the full FDA submission: accessdata.fda.gov

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IPS 99 ONE AND IPS 99 CERAM

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