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Fs Disposable Interface 660065AN

by Johnson & Johnson Surgical Vision, Inc.

Fs Disposable Interface 660065AN is a Class I device made by Johnson & Johnson Surgical Vision, Inc., listed in FDA GUDID since 2 Sep 2016 (UDI-DI 05050474535305), 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 Number05050474535305 UDI-DI Date2 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  • Withdrawn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
Fs Disposable Interface
Generic name
Laser beam delivery unit holder
Model / Ref / Catalog
660065AN
Primary DI / UDI-DI
05050474535305
FDA product code
HNO, GEX
GMDN term
Laser beam delivery unit holder
Device class
Class I
Regulation number
886.4370, 878.4810
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HNO (KERATOME, AC-POWERED).

Other devices from Johnson & Johnson Surgical Vision, Inc.

See all devices from Johnson & Johnson Surgical Vision, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)