K-number	K103391
Device name	IVOBASE HYBRID, IVOBASE HIGH IMPACT
Applicant	Ivoclar Vivadent, Inc.
Product code	EBI
Device class	Class II
Decision date	Feb 17, 2011
Decision	Substantially Equivalent
Regulation	872.3760

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View the full FDA submission: accessdata.fda.gov

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IVOBASE HYBRID, IVOBASE HIGH IMPACT

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