K-number	K252845
Device name	Venus Nova (FP-2001)
Applicant	Venus Concept, Inc.
Product code	GEI
Device class	Class II
Decision date	Nov 6, 2025
Decision	Substantially Equivalent
Regulation	—

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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Venus Nova (FP-2001)

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