K-number	K150296
Device name	Biodenta Customized Abutment-Hybrid
Applicant	Biodenta Swiss AG
Product code	NHA
Device class	Class II
Decision date	Jul 2, 2015
Decision	Substantially Equivalent
Regulation	872.3630

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View the full FDA submission: accessdata.fda.gov

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Biodenta Customized Abutment-Hybrid

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