K-number	K132984
Device name	SR VIVODENT S, SR ORTHOTYP S, SR ORTHOLINGUAL S
Applicant	Ivoclar Vivadent, Inc.
Product code	ELM
Device class	Class II
Decision date	Jan 14, 2014
Decision	Substantially Equivalent
Regulation	872.3590

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View the full FDA submission: accessdata.fda.gov

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SR VIVODENT S, SR ORTHOTYP S, SR ORTHOLINGUAL S

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