K-number	K222688
Device name	The Trust
Applicant	Genoss Co., Ltd.
Product code	EKX
Device class	Class I
Decision date	Aug 9, 2024
Decision	Substantially Equivalent
Regulation	872.4200

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Source

View the full FDA submission: accessdata.fda.gov

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The Trust

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