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Medical Face Shield DF-20

by Denjoy Dental Co., Ltd

Medical Face Shield DF-20 is a Class I device made by Denjoy Dental Co., Ltd, listed in FDA GUDID since 19 Feb 2022 (UDI-DI 06970873260280), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06970873260280 UDI-DI Date19 Feb 2022ListedStatusListed 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  • Withdrawn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
Medical Face Shield
Generic name
Face splash shield, single-use
Model / reference
DF-20
Primary DI / UDI-DI
06970873260280
FDA product code
LYU
GMDN term
Face splash shield, single-use
Device class
Class I
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LYU (Accessory, Surgical Apparel).

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)