K-number	K242389
Device name	EyeGility Inserter for Preloaded enVista IOLs
Applicant	Bausch & Lomb, Incorporated
Product code	MSS
Device class	Class I
Decision date	Oct 10, 2024
Decision	Substantially Equivalent
Regulation	886.4300

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Source

View the full FDA submission: accessdata.fda.gov

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EyeGility Inserter for Preloaded enVista IOLs

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EyeGility Inserter for Preloaded enVista IOLs