Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004860474

FEI Number

3004860474

Entity Name

HELTON INC

City/State/Country

Morrison, TN, US

Establishment Address

8700 Manchester Hwy, Morrison, TN 37357, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Helton Inc (Owner Number: 10087957)

Owner / Operator Contact Address

8700 Manchester Hwy, Morrison, TN 37357, US

Initial Importer Flag

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
FNJ	Bed, Manual	General Hospital	Class 1	880.5120	2023-05-05

Official Correspondent

Chris Helton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Helton 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 3004860474. Last updated year: 2026. Please use registration number 3004860474 when referencing this establishment in official correspondence.