Skip to content

ASSI.FOHL22326

by Accurate Surgical & Scientific Instruments Corp.

ASSI.FOHL22326 is a Class II device made by Accurate Surgical & Scientific Instruments Corp., listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00841645132004), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841645132004 UDI-DI Date26 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  • Withdrawn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
Assi
Generic name
Head-worn fibreoptic light
Model / reference
ASSI.FOHL22326
Description
Fiber Optic Headlight with Cable 3.5mm dia. F/O Cable, Dbl. Lens System Adjustable Cushioned Headband
Primary DI / UDI-DI
00841645132004
FDA product code
FCT
GMDN term
Head-worn fibreoptic light
Device class
Class II
Regulation number
886.4335
GUDID distribution status
In Commercial Distribution
Sterilisation method
Liquid Chemical

Similar devices

Other devices filed under FDA product code FCT (Headlight, Fiberoptic Focusing).

Other devices from Accurate Surgical & Scientific Instruments Corp.

See all devices from Accurate Surgical & Scientific Instruments Corp. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)