KLEEN TEST PRODUCTS CORPORATION

FDA Device Registration & Listing · Port Washington, WI, US · Registration 3004586080

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
3004586080
FEI Number
3004586080
Entity Name
KLEEN TEST PRODUCTS CORPORATION
City/State/Country
Port Washington, WI, US
Establishment Address
1611 S SUNSET RD, Port Washington, WI 53074, 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
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
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2015-05-15

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.
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Other Registrations for Same Entity

Registration Number Establishment Name Location
1526481 KLEEN TEST PRODUCTS CORPORATION Strasburg, OH, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004586080. Last updated year: 2026. Please use registration number 3004586080 when referencing this establishment in official correspondence.
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