K-number	K220003
Device name	EzOrtho v1.3
Applicant	Ewoosoft Co., Ltd.
Product code	LLZ
Device class	Class II
Decision date	Feb 23, 2022
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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EzOrtho v1.3

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