Contract manufacturerMORGAN NEWTON COMPANY (Plano, TX)TexasNeurologyOphthalmicClass IIClass I
MORGAN NEWTON COMPANY
Contract manufacturer · Plano, TX
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3008312728 (openFDA record; or search FDA's registration database)
- FEI number
- 3008312728
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Morgan Newton Company (FDA owner/operator no. 10059741)
- Registered address
- 3401 Wynwood Drive, Plano, TX 75074
- Contract listings
- 5 device listings, 4 product codes, first listed Feb 18, 2019
- 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 code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| GXY | Electrode, Cutaneous | Class II | Neurology | Contract manufacturing | Apr 3, 2020 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | Class II | Neurology | Contract manufacturing | Feb 18, 2019 |
| HPT | Perimeter, Automatic, Ac-Powered | Class I | Ophthalmic | Contract manufacturing | Aug 1, 2024 |
| QJQ | Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety | Class II | Neurology | Contract manufacturing | Feb 18, 2019 |