Contract manufacturerAR FABRICATING (Georgetown, TX)TexasOrthopedicClass II
AR FABRICATING
Contract manufacturer · Georgetown, TX
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3010143171 (openFDA record; or search FDA's registration database)
- FEI number
- 3010143171
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- AR Fabricating (FDA owner/operator no. 10043437)
- Registered address
- 40132 Industrial Park Cir Ste 102, Georgetown, TX 78626
- Contract listings
- 6 device listings, 6 product codes, first listed Jan 24, 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 |
|---|---|---|---|---|---|
| KWP | Appliance, Fixation, Spinal Interlaminal | Class II | Orthopedic | Contract manufacturing | Feb 4, 2026 |
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Class II | Orthopedic | Contract manufacturing | Feb 4, 2026 |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Class II | Orthopedic | Contract manufacturing | Jan 24, 2019 |
| NKB | Thoracolumbosacral Pedicle Screw System | Class II | Orthopedic | Contract manufacturing | Feb 4, 2026 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | Class II | Orthopedic | Contract manufacturing | Jan 24, 2019 |
| OUR | Sacroiliac Joint Fixation | Class II | Orthopedic | Contract manufacturing | Feb 4, 2026 |