Contract manufacturerSINTX Technologies Inc. (Salt Lake City, UT)UtahOrthopedicClass II
SINTX Technologies Inc.
Contract manufacturer ยท Salt Lake City, UT
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3005032068 (openFDA record; or search FDA's registration database)
- FEI number
- 3005032068
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Manufacturer; Contract manufacturer
- Owner or operator
- SINTX Technologies (FDA owner/operator no. 9071516)
- Registered address
- 1885 W 2100 S, Salt Lake City, UT 84119
- Contract listings
- 2 device listings, 3 product codes, first listed Feb 22, 2008
- 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 |
|---|---|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Class II | Orthopedic | Contract manufacturing | Jan 2, 2015 |
| MQP | Spinal Vertebral Body Replacement Device | Class II | Orthopedic | Contract manufacturing | Feb 22, 2008 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | Class II | Orthopedic | Contract manufacturing | Jan 2, 2015 |