CoolGlide Vantage

by Cutera, Inc.

CoolGlide Vantage is a Class II device made by Cutera, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00816722021021), registry data as of 31 May 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 31 May 2026.

Regulatory status

as of registry sync 31 May 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00816722021021 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00816722021021

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Dermatological solid-state laser system
Model / reference: CoolGlide Vantage

Primary DI / UDI-DI: 00816722021021
FDA product code: GEX
GMDN term: Dermatological solid-state laser system

Device class: Class II
Regulation number: 878.4810
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Serial number
Manufacturing date

Other properties (12, all answered No)