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Virtual Field VF3 Pro

by VIRTUAL FIELD, Inc

Virtual Field VF3 Pro is a Class I device made by VIRTUAL FIELD, Inc, listed in FDA GUDID since 23 Jan 2023 (UDI-DI 00860001720402), 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 Number00860001720402 UDI-DI Date23 Jan 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  • Withdrawn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
Virtual Field
Generic name
Pupil-size/-light reflex meter
Model / reference
VF3 Pro
Primary DI / UDI-DI
00860001720402
FDA product code
HPT, HRI, HIT
GMDN term
Pupil-size/-light reflex meter
Device class
Class I
Regulation number
886.1605, 886.1690, 886.1170
GUDID distribution status
In Commercial Distribution

Related devices

Category: Perimeter, automaticPupillographColour discrimination testerPupillometer, electrically-powered

Similar devices

Other devices filed under FDA product code HPT (Perimeter, Automatic, Ac-Powered).

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Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)