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Titan V

by Cutera, Inc.

Titan V is a Class II device made by Cutera, Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00816722022905), registry data as of 8 Jun 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

Unverified

Source GUDID, synced 8 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816722022905 UDI-DI Date19 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Dermatological laser beam guiding handpiece
Model / reference
Titan V
Primary DI / UDI-DI
00816722022905
FDA product code
ILY
GMDN term
Dermatological laser beam guiding handpiece
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dermatological laser beam guiding handpiece

Similar devices in this category

Other devices filed under Dermatological laser beam guiding handpiece.

Other devices from Cutera, Inc.

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    Class II

  • CoolView

    Class II

  • AviClear

    Class II

  • Solera Opus

    Class II

See all devices from Cutera, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)