Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033274169

FEI Number

3033274169

Entity Name

HARDY MANUFACTURING

City/State/Country

Decatur, GA, US

Establishment Address

2467 Ridgefield Ter, Decatur, GA 30033, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Hardy Manufacturing (Owner Number: 10091869)

Owner / Operator Contact Address

2467 Ridgefield Terrace, Decatur, GA 30033, 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
LXM	Manipulator, Plunger-Like Joint	Unknown	Class U	N/A	2024-11-10

Official Correspondent

Glen Hardy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hardy Manufacturing

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 3033274169. Last updated year: 2026. Please use registration number 3033274169 when referencing this establishment in official correspondence.