K-number	K223173
Device name	Proxeo ULTRA (PB-510, PB-520 and PB-530)
Applicant	W&H Dentalwerk Buermoss GmbH
Product code	ELC
Device class	Class II
Decision date	Jul 14, 2023
Decision	Substantially Equivalent
Regulation	872.4850

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View the full FDA submission: accessdata.fda.gov

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Proxeo ULTRA (PB-510, PB-520 and PB-530)

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