MedtechSourcebook

Core Products International Inc

Contract manufacturer · Chetek, WI

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

FDA registration
3008008970 (openFDA record; or search FDA's registration database)
FEI number
3008008970
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer; Repackager or relabeler
Owner or operator
Core Products International, Inc. (FDA owner/operator no. 9002815)
Registered address
1505 Parker Drive, Chetek, WI 54728
Contract listings
10 device listings, 10 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
BYIPercussor, Powered-ElectricClass IIAnesthesiologyContract manufacturingJun 14, 2022
FSDBinder, AbdominalClass IGeneral hospitalContract manufacturingDec 15, 2010
HSTApparatus, Traction, Non-PoweredClass IOrthopedicContract manufacturingDec 15, 2010
ILISling, ArmClass IPhysical medicineContract manufacturingSep 21, 2006
ILZAccessories, TractionClass IPhysical medicineContract manufacturingDec 15, 2010
IMEPack, Hot Or Cold, ReusableClass IPhysical medicineContract manufacturingSep 21, 2006
IQIOrthosis, Limb BraceClass IPhysical medicineContract manufacturingSep 21, 2006
IQKOrthosis, CervicalClass IPhysical medicineContract manufacturingMay 16, 2016
ITQJoint, Knee, External BraceClass IPhysical medicineContract manufacturingDec 15, 2010
MRIOrthosis, Truncal/Orthosis, LimbClass IPhysical medicineContract manufacturingSep 21, 2006

Other contract facilities of Core Products International, Inc.