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Optitek 7259-125

by Diversified Products, Inc.

Optitek 7259-125 is a Class I device made by Diversified Products, Inc., listed in FDA GUDID since 28 Nov 2022 (UDI-DI 00842894171844), 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 Number00842894171844 UDI-DI Date28 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  • Withdrawn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
Optitek
Generic name
Magnifying spectacles
Model / reference
7259-125
Primary DI / UDI-DI
00842894171844
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

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)