K-number	K200586
Device name	Straumann TLX Implant System
Applicant	Institut Straumann AG
Product code	DZE
Device class	Class II
Decision date	Aug 20, 2020
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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Straumann TLX Implant System

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