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iTOVi ITS31

by Itovi, LLC

iTOVi ITS31 is a Class II device made by Itovi, LLC, listed in FDA GUDID since 4 Sep 2019 (UDI-DI 00866387000411), 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 Number00866387000411 UDI-DI Date4 Sep 2019ListedStatusListed 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  • Withdrawn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
iTOVi
Generic name
Skin electrical conductance meter
Model / reference
ITS31
Primary DI / UDI-DI
00866387000411
FDA product code
GZO
GMDN term
Skin electrical conductance meter
Device class
Class II
Regulation number
882.1540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin electrical conductance meter

Similar devices

Other devices filed under FDA product code GZO (Device, Galvanic Skin Response Measurement).

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)