K-number	K213149
Device name	VOCO Retraction Paste
Applicant	Voco GmbH
Product code	MVL
Device class	Class U
Decision date	Dec 9, 2021
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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VOCO Retraction Paste

Everything you need for a 510(k) submission. Nothing you don't.