EEG Software LLC

FDA Device Registration & Listing · Gainesville, FL, US · Registration 3010129717

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
3010129717
FEI Number
3010129717
Entity Name
EEG Software LLC
City/State/Country
Gainesville, FL, US
Establishment Address
2603 NW 13th Street, #138, Gainesville, FL 32609, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
EEG Software LLC (Owner Number: 10043501)
Owner / Operator Contact Address
2603 NW 13th Street, #138, Gainesville, FL 32609, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K122879
PMA Number
N/A

All Registered Proprietary Names

EEGer EEGer4

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2013-02-21

Official Correspondent

Karin Lightstone

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EEG Software LLC
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
K873418 Bodylog, Inc. BODYLOG STRESS REDUCTION PACKAGE 1987-12-17
K792659 Bio-Feedback Systems, Inc. FEEDBACK EDR SYSTEM MODEL ME-1 1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010129717. Last updated year: 2026. Please use registration number 3010129717 when referencing this establishment in official correspondence.
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