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Clarity II Assy_holder_window

by Lutronic Corporation

Clarity II Assy_holder_window is a Class II device made by Lutronic Corporation, listed in FDA GUDID since 16 Jun 2020 (UDI-DI 08809447652528), registry data as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809447652528 UDI-DI Date16 Jun 2020ListedStatusListed 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  • Withdrawn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

Trade name
Clarity II
Generic name
Dermatological solid-state laser system
Model / reference
ASSY_HOLDER_WINDOW
Primary DI / UDI-DI
08809447652528
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

Related devices

Category: Dermatological solid-state laser system

Similar devices in this category

Other devices filed under Dermatological solid-state laser system.

Other devices from Lutronic Corporation

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Properties

  • Prescription use
Other properties (14, all answered No)