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Virtual Eye Software 3.2.0

by Virtual Vision Health

Virtual Eye Software 3.2.0 (VV-021) is a Class I device made by Virtual Vision Health, listed in FDA GUDID since 16 Dec 2024 (UDI-DI 00860010709795), 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 Number00860010709795 UDI-DI Date16 Dec 2024ListedStatusListed 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  • Withdrawn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 Eye Software
Generic name
Perimeter, automatic
Model / Ref / Catalog
3.2.0, VV-021
Primary DI / UDI-DI
00860010709795
FDA product code
HIT, HRI, HPT
GMDN term
Perimeter, automatic
Device class
Class I
Regulation number
886.1170, 886.1690, 886.1605
GUDID distribution status
In Commercial Distribution

Related devices

Category: Perimeter, automatic

Similar devices in this category

Other devices filed under Perimeter, automatic.

Other devices from Virtual Vision Health

See all devices from Virtual Vision Health →

Properties

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