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Yoshitomi Meibomian Gland Compressor Ae-4521

by Katena Products, Inc.

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 22 Oct 2026. What this means

Overview

A hand-held manual instrument designed for non-dedicated grasping of devices, sponges and/or dressings during a procedure. Reusable, available in various sizes, made of metal or plastic materials.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841668135716 UDI-DI Date7 Dec 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  • Withdrawn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
Yoshitomi Meibomian Gland Compressor
Generic Name
Dressing/utility forceps, tweezers-like, reusable
Model / Ref / Catalog
AE-4521
Primary DI / UDI-DI
00841668135716
FDA Product Code
HNR
GMDN Term
Dressing/utility forceps, tweezers-like, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dressing/utility forceps, tweezers-like, reusable

Other devices from Katena Products, Inc.

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Properties

  • Prescription Use
  • Premarket Exempt

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: 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