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NeuroMatch 1.0.4

by LVIS Corporation

NeuroMatch 1.0.4 is a Class II device made by LVIS Corporation, listed in FDA GUDID since 4 Apr 2025 (UDI-DI 00850056774000), 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 Number00850056774000 UDI-DI Date4 Apr 2025ListedStatusListed 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  • Withdrawn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
NeuroMatch
Generic name
Bioelectrical signal analysis software
Model / reference
1.0.4
Primary DI / UDI-DI
00850056774000
FDA product code
OMB, OMA, OLT
GMDN term
Bioelectrical signal analysis software
Device class
Class II
Regulation number
882.1400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bioelectrical signal analysis software

Similar devices

Other devices filed under FDA product code OMB (Automatic Event Detection Software For Full-Montage Electroencephalograph).

Other devices from LVIS Corporation

  • NeuroMatch 1.0.7

    Class II

  • LVIS NeuroMatch

    Class II

  • NeuroMatch

    Class II

  • NeuroMatch

    Class II

Properties

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