K-number	K103773
Device name	ZENOFLEX DIMENSION
Applicant	Wieland Dental + Technik GmbH & Co. KG
Product code	EIH
Device class	Class II
Decision date	Mar 16, 2011
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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ZENOFLEX DIMENSION

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