K-number	K243968
Device name	Revolve Surgical System
Applicant	Revolve Surgical, Inc.
Product code	GCJ
Device class	Class II
Decision date	Oct 3, 2025
Decision	Substantially Equivalent
Regulation	876.1500

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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Revolve Surgical System

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