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Optego 98872

by Optego Vision USA, Inc.

Optego 98872 is a Class I device made by Optego Vision USA, Inc., listed in FDA GUDID since 15 Sep 2023 (UDI-DI 00360843010728), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00360843010728 UDI-DI Date15 Sep 2023ListedStatusListed 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  • Withdrawn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
Optego
Generic name
Vision testing/training chart
Model / reference
98872
Primary DI / UDI-DI
00360843010728
FDA product code
HOX
GMDN term
Vision testing/training chart
Device class
Class I
Regulation number
886.1150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vision testing/training chart

Similar devices in this category

Other devices filed under Vision testing/training chart.

Other devices from Optego Vision USA, Inc.

See all devices from Optego Vision USA, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)