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Optego 936703

by Optego Vision USA, Inc.

Optego 936703 is a Class I device made by Optego Vision USA, Inc., listed in FDA GUDID since 1 Nov 2023 (UDI-DI 00360843010261), 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 Number00360843010261 UDI-DI Date1 Nov 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  • Withdrawn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
Diagnostic ophthalmic prism
Model / reference
936703
Primary DI / UDI-DI
00360843010261
FDA product code
HKW
GMDN term
Diagnostic ophthalmic prism
Device class
Class I
Regulation number
886.1650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Diagnostic ophthalmic prism

Other devices from Optego Vision USA, Inc.

See all devices from Optego Vision USA, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)