K-number	K233077
Device name	FlashHeal 2 (FlashHeal 2.0)
Applicant	Inwound Aps
Product code	GEX
Device class	Class II
Decision date	Jan 18, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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FlashHeal 2 (FlashHeal 2.0)

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