MedtechSourcebook

KLEEN TEST PRODUCTS CORPORATION

Contract manufacturer · Port Washington, WI

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration
3004586080 (openFDA record; or search FDA's registration database)
FEI number
3004586080
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
KLEEN TEST PRODUCTS CORPORATION (FDA owner/operator no. 2122794)
Registered address
1611 S SUNSET RD, Port Washington, WI 53074
Contract listings
1 device listings, 1 product codes, first listed May 15, 2015
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
FRLFiber, Medical, AbsorbentClass IGeneral hospitalContract manufacturingMay 15, 2015

Other contract facilities of KLEEN TEST PRODUCTS CORPORATION