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Clear Readers 1080-125

by Diversified Products, Inc.

Clear Readers 1080-125 is a Class I device made by Diversified Products, Inc., listed in FDA GUDID since 19 Nov 2022 (UDI-DI 00842894127216), 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 Number00842894127216 UDI-DI Date19 Nov 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  • Withdrawn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
Clear Readers
Generic name
Magnifying spectacles
Model / reference
1080-125
Primary DI / UDI-DI
00842894127216
FDA product code
HOI
GMDN term
Magnifying spectacles
Device class
Class I
Regulation number
886.5840
GUDID distribution status
In Commercial Distribution

Related devices

Category: Magnifying spectacles

Similar devices

Other devices filed under FDA product code HOI (Spectacle, Magnifying).

Other devices from Diversified Products, Inc.

See all devices from Diversified Products, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)