Data / Medical devices / United States / Lvis Corporation

Lvis Corporation: FDA-registered device maker in Palo Alto, CA, United States, 3 510(k) clearances

Name: Lvis Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Lvis Corporation is registered with the FDA (registration 3015929663) in Palo Alto, CA, United States. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 23, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3015929663
Address: 2600 E Bayshore Road, Palo Alto, CA, United States, 94303
Owner or operator: LVIS Corporation (10090414)
Roles: Complaint file establishment, Manufacturer
First device listed: March 25, 2024
Registered through: 2026
Brand names listed: NeuroMatch

Devices it lists

Device	Product code	Class	Role	Source
Amplitude-Integrated Electroencephalograph	OMA	2	Complaint file establishment, Manufacturer	accessdata.fda.gov
Automatic Event Detection Software For Full-Montage Electroencephalograph	OMB	2	Complaint file establishment, Manufacturer	accessdata.fda.gov
Non-Normalizing Quantitative Electroencephalograph Software	OLT	2	Complaint file establishment, Manufacturer	accessdata.fda.gov
Source Localization Software For Electroencephalograph Or Magnetoencephalograph	OLX	2	Complaint file establishment, Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
May 23, 2025	K250239	NeuroMatch	OLX	Substantially Equivalent	LVIS Corporation	accessdata.fda.gov
November 26, 2024	K241390	NeuroMatch	OMB	Substantially Equivalent	LVIS Corporation	accessdata.fda.gov
June 9, 2023	K222450	LVIS NeuroMatch	OMB	Substantially Equivalent	LVIS Corporation	accessdata.fda.gov

Compare with other makers

Updated May 23, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.