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StaticVR V1

by Virtualis

StaticVR V1 is a Class I device made by Virtualis, listed in FDA GUDID since 9 Dec 2021 (UDI-DI 03760310780555), 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 Number03760310780555 UDI-DI Date9 Dec 2021ListedStatusListed 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  • Withdrawn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
StaticVR
Generic name
Posturography system platform
Model / reference
V1
Primary DI / UDI-DI
03760310780555
FDA product code
KHX
GMDN term
Posturography system platform
Device class
Class I
Regulation number
890.1575
GUDID distribution status
In Commercial Distribution

Related devices

Category: Posturography system platform

Similar devices

Other devices filed under FDA product code KHX (Platform, Force-Measuring).

Other devices from Virtualis

See all devices from Virtualis →

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)