Contract manufacturerTecomet, Inc. (Wilmington, MA)MassachusettsOrthopedicClass II
Tecomet, Inc.
Contract manufacturer ยท Wilmington, MA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3005226664 (openFDA record; or search FDA's registration database)
- FEI number
- 3005226664
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Tecomet (FDA owner/operator no. 10031319)
- Registered address
- 301 Ballardvale St, Wilmington, MA 01887
- Contract listings
- 10 device listings, 6 product codes, first listed May 1, 2017
- 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 | May 1, 2017 |
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Class II | Orthopedic | Contract manufacturing | May 1, 2017 |
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | Class II | Orthopedic | Contract manufacturing | May 1, 2017 |
| MNI | Orthosis, Spinal Pedicle Fixation | Class II | Orthopedic | Contract manufacturing | May 1, 2017 |
| NKB | Thoracolumbosacral Pedicle Screw System | Class II | Orthopedic | Contract manufacturing | May 1, 2017 |
| NKG | Posterior Cervical Screw System | Class II | Orthopedic | Contract manufacturing | May 1, 2017 |