MedtechSourcebook

ARxIUM, INC.

Contract manufacturer ยท Buffalo Grove, IL

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

FDA registration
3012205369 (openFDA record; or search FDA's registration database)
FEI number
3012205369
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
ARxIUM, Inc. (FDA owner/operator no. 9094339)
Registered address
1000 Asbury Drive, Suite 4, Buffalo Grove, IL 60089
Contract listings
1 device listings, 1 product codes, first listed Nov 6, 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
NEPSystem/Device, Pharmacy CompoundingClass IIGeneral hospitalContract manufacturingNov 6, 2006