AIONEX, INC.

FDA Device Registration & Listing · Madison, TN, US · Registration 3005627440

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
3005627440
FEI Number
3005627440
Entity Name
AIONEX, INC.
City/State/Country
Madison, TN, US
Establishment Address
122 Cude Lane, Madison, TN 37115, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AIONEX, INC. (Owner Number: 9083665)
Owner / Operator Contact Address
122 Cude Lane, Madison, TN 37115, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Aionex Patient Communication System (ADVOCATE nurse call)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILQ System, Communication, Powered Physical Medicine Class 2 890.3710 2006-03-01

Official Correspondent

CURT FREEMYER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0004-2016 Lifeline Systems, Incorporated 2
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005627440. Last updated year: 2026. Please use registration number 3005627440 when referencing this establishment in official correspondence.
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