VISPALEXO, INC

FDA Device Registration & Listing · North Canton, OH, US · Registration 3039260720

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
3039260720
FEI Number
3039260720
Entity Name
VISPALEXO, INC
City/State/Country
North Canton, OH, US
Establishment Address
4305 Mount Pleasant St Nw Ste 203b, North Canton, OH 44720, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
VispalExo, Inc (Owner Number: 10093848)
Owner / Operator Contact Address
4305 Mount Pleasant St., NW, Suite 203B, North Canton, OH 44720, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2025-07-22

Official Correspondent

Michael Funk

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VispalExo, Inc
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 3039260720. Last updated year: 2026. Please use registration number 3039260720 when referencing this establishment in official correspondence.
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