Skip to content

Vortex Surgical Inc VS0800

by Vortex Surgical, Inc.

Vortex Surgical Inc VS0800 is an ophthalmic fibreoptic light instrument (FDA Class I; FDA product code HNX, Depressor, Orbital) made by Vortex Surgical, Inc., listed in FDA GUDID since 1 Feb 2023 (UDI-DI 00810123481699), 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 Number00810123481699 UDI-DI Date1 Feb 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  • Withdrawn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
Vortex Surgical Inc
Generic name
Ophthalmic fibreoptic light instrument, single-use
Model / reference
VS0800
Primary DI / UDI-DI
00810123481699
FDA product code
HNX
GMDN term
Ophthalmic fibreoptic light instrument, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic fibreoptic light instrument, single-use

Similar devices in this category

Other devices filed under Ophthalmic fibreoptic light instrument, single-use.

Other devices from Vortex Surgical, Inc.

See all devices from Vortex Surgical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)