NEUROFIELD, INC.

FDA Device Registration & Listing · Santa Barbara, CA, US · Registration 3010900508

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
3010900508
FEI Number
3010900508
Entity Name
NEUROFIELD, INC.
City/State/Country
Santa Barbara, CA, US
Establishment Address
1836 State St, Santa Barbara, CA 93101, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Neurofield, Inc. (Owner Number: 10046907)
Owner / Operator Contact Address
1836 State Street, Santa Barbara, CA 93101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Genesis Q-Check

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QJQ Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety Neurology Class 2 882.5800 2026-05-04
GYA Tester, Electrode/Lead, Electroencephalograph Neurology Class 1 882.1410 2023-12-20

Official Correspondent

Nicholas Dogris

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010900508. Last updated year: 2026. Please use registration number 3010900508 when referencing this establishment in official correspondence.
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