K-number	K191256
Device name	Straumann BLX Ø3.5 mm Implants
Applicant	Institut Straumann AG
Product code	DZE
Device class	Class II
Decision date	Dec 27, 2019
Decision	Substantially Equivalent
Regulation	872.3640

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Source

View the full FDA submission: accessdata.fda.gov

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Straumann BLX Ø3.5 mm Implants

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