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Retractable ILM Elevator 23ga

by Vortex Surgical, Inc.

Retractable ILM Elevator 23ga (VS0350.23) is a general-purpose ophthalmic hook (FDA Class I; FDA product code HNQ, Hook, Ophthalmic) made by Vortex Surgical, Inc., listed in FDA GUDID since 9 Mar 2018 (UDI-DI B384VS0350231), 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 NumberB384VS0350231 UDI-DI Date9 Mar 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Retractable ILM Elevator
Generic name
General-purpose ophthalmic hook, single-use
Model / Ref / Catalog
23ga, VS0350.23
Primary DI / UDI-DI
B384VS0350231
FDA product code
HNQ
GMDN term
General-purpose ophthalmic hook, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose ophthalmic hook, single-use

Similar devices

Other devices filed under FDA product code HNQ (Hook, Ophthalmic).

Other devices from Vortex Surgical, Inc.

See all devices from Vortex Surgical, Inc. →

Properties

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