MedtechSourcebook

CO-AX TECHNOLOGY, INC.

Contract manufacturer ยท Solon, OH

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

2021Product codes first listed, by year (tallest: 2)2026
FDA registration
3013413442 (openFDA record; or search FDA's registration database)
FEI number
3013413442
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
CO-AX Technology, Inc. (FDA owner/operator no. 10053576)
Registered address
30301 Emerald Valley Pkwy, Solon, OH 44139
Contract listings
1 device listings, 2 product codes, first listed Aug 13, 2021
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
GWQFull-Montage Standard ElectroencephalographClass IINeurologyContract manufacturingAug 13, 2021
HCCDevice, BiofeedbackClass IINeurologyContract manufacturingAug 13, 2021