K-number	K232350
Device name	Stryker Facial iD System
Applicant	Stryker Craniomaxillofacial
Product code	JEY
Device class	Class II
Decision date	Jan 13, 2024
Decision	Substantially Equivalent
Regulation	872.4760

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Source

View the full FDA submission: accessdata.fda.gov

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Stryker Facial iD System

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