Skip to content

Alcon 749590397175

by Alcon Laboratories, Inc.

Alcon 749590397175 is a vision testing/training flipper (FDA Class I) made by Alcon Laboratories, Inc., listed in FDA GUDID since 19 Oct 2021 (UDI-DI 00749590397175), 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 Number00749590397175 UDI-DI Date19 Oct 2021ListedStatusListed 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  • Withdrawn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
Alcon
Generic name
Vision testing/training flipper
Model / reference
749590397175
Primary DI / UDI-DI
00749590397175
FDA product code
HPC, HPA
GMDN term
Vision testing/training flipper
Device class
Class I
Regulation number
886.1405, 886.1415
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vision testing/training flipper

Similar devices

Other devices filed under FDA product code HPC (Set, lens, trial, ophthalmic).

Other devices from Alcon Laboratories, Inc.

See all devices from Alcon Laboratories, Inc. →

Properties

  • Premarket exempt
  • Expiration date
Other properties (13, all answered No)