K-number	K211427
Device name	CREOKORREKT Aligners
Applicant	Creodent Prosthetics, Ltd.
Product code	NXC
Device class	Class II
Decision date	Oct 13, 2022
Decision	Substantially Equivalent
Regulation	872.5470

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Source

View the full FDA submission: accessdata.fda.gov

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CREOKORREKT Aligners

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