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Spectacle Frame LXGL

by Luxin Optical (Shanghai) Co., Ltd.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number16974852470018 UDI-DI Date9 Mar 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Spectacle Frame
Generic Name
Prescription spectacles
Model / Reference
LXGL
Primary DI / UDI-DI
16974852470018
FDA Product Code
HQZ
GMDN Term
Prescription spectacles
Device Class
Class I
Regulation Number
886.5842
GUDID distribution status
In Commercial Distribution

Related devices

Category: Prescription spectacles

Other devices from Luxin Optical (Shanghai) Co., Ltd.

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No