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Alcon 8065751051

by Alcon Laboratories, Inc.

Alcon 8065751051 is a Class II device made by Alcon Laboratories, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00380657510511), 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 Number00380657510511 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Laser adaptor
Model / reference
8065751051
Primary DI / UDI-DI
00380657510511
FDA product code
HQF
GMDN term
Laser adaptor
Device class
Class II
Regulation number
886.4390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laser adaptor

Similar devices

Other devices filed under FDA product code HQF (Laser, ophthalmic).

Other devices from Alcon Laboratories, Inc.

See all devices from Alcon Laboratories, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)