LVIS CORPORATION

FDA Device Registration & Listing · Palo Alto, CA, US · Registration 3015929663

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015929663
FEI Number
3015929663
Entity Name
LVIS CORPORATION
City/State/Country
Palo Alto, CA, US
Establishment Address
2600 E Bayshore Road, Palo Alto, CA 94303, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
LVIS Corporation (Owner Number: 10090414)
Owner / Operator Contact Address
2600 E Bayshore Road, Palo Alto, CA 94303, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

NeuroMatch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OMB Automatic Event Detection Software For Full-Montage Electroencephalograph Neurology Class 2 882.1400 2025-06-05
OLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph Neurology Class 2 882.1400 2025-06-05
OMA Amplitude-Integrated Electroencephalograph Neurology Class 2 882.1400 2025-06-05
OLT Non-Normalizing Quantitative Electroencephalograph Software Neurology Class 2 882.1400 2025-06-05

Official Correspondent

Sweta Srivastava

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LVIS Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K033010 Brainz Instruments , Ltd. BRM2 BRAIN MONITOR 2003-10-10
K991012 Siemens Medical Solutions USA, Inc. SIEMENS INFINITY EEG POD 1999-06-24
K852587 Tracor Northern, Inc. CDSA(COLOR DENSITY, SPECTRAL ARRRAY) 1985-08-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015929663. Last updated year: 2026. Please use registration number 3015929663 when referencing this establishment in official correspondence.
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