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Kazuo Kawasaki MP-121 13 BRN 50

by Masunaga Optical Mfg.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

Overview

Discover the Kazuo Kawasaki spectacle frame, a highly advanced ophthalmic device designed to provide exceptional comfort and clarity for users. This cutting-edge device features a sturdy plastic or metallic frame that securely holds a pair of prescription lenses in front of the eyes, promoting optimal vision and reducing eye strain. With its durable design and adjustable fit, this spectacles frame is ideal for individuals seeking improved visual acuity.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04582644469529 UDI-DI Date26 Apr 2022ListedStatusListed 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  • Withdrawn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
Kazuo Kawasaki
Generic Name
Spectacle frame
Model / Reference
MP-121 13 BRN 50
Primary DI / UDI-DI
04582644469529
FDA Product Code
HQZ
GMDN Term
Spectacle frame
Device Class
Class I
Regulation Number
886.5842
GUDID distribution status
In Commercial Distribution

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Properties

  • Premarket Exempt

Other properties (13)

  • 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
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No