MedtechSourcebook

CORE PRODUCTS INTL., INC.

Contract manufacturer · Osceola, WI

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

FDA registration
2183988 (openFDA record; or search FDA's registration database)
FEI number
1000115743
Registered for
FDA registration year 2026
Establishment types
Specification developer; Manufacturer; Contract manufacturer
Owner or operator
Core Products International, Inc. (FDA owner/operator no. 9002815)
Registered address
808 PROSPECT AVE., Osceola, WI 54020
Contract listings
2 device listings, 2 product codes, first listed Sep 21, 2006
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
IQKOrthosis, CervicalClass IPhysical medicineContract manufacturingMay 16, 2016
MRIOrthosis, Truncal/Orthosis, LimbClass IPhysical medicineContract manufacturingSep 21, 2006

Other contract facilities of Core Products International, Inc.