Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1526481

FEI Number

1526481

Entity Name

KLEEN TEST PRODUCTS CORPORATION

City/State/Country

Strasburg, OH, US

Establishment Address

216 12TH ST NE, Strasburg, OH 44680, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

KLEEN TEST PRODUCTS CORPORATION (Owner Number: 2122794)

Owner / Operator Contact Address

1611 SUNSET RD., --, Port Washington, WI 53074, 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
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2013-11-06

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KLEEN TEST PRODUCTS CORPORATION

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3004586080	KLEEN TEST PRODUCTS CORPORATION	Port Washington, WI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1526481. Last updated year: 2026. Please use registration number 1526481 when referencing this establishment in official correspondence.