Contract manufacturerALLOSOURCE (Centennial, CO)ColoradoGeneral and plastic surgeryNeurologyOrthopedicClass II
ALLOSOURCE
Contract manufacturer ยท Centennial, CO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3000215346 (openFDA record; or search FDA's registration database)
- FEI number
- 3000215346
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- AlloSource (FDA owner/operator no. 10025681)
- Registered address
- 6278 S Troy Circle, Centennial, CO 80111
- Contract listings
- 8 device listings, 5 product codes, first listed Jun 29, 2011
- 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 |
|---|---|---|---|---|---|
| FTM | Mesh, Surgical | Class II | General and plastic surgery | Contract manufacturing | Jul 21, 2020 |
| JXI | Cuff, Nerve | Class II | Neurology | Contract manufacturing | Dec 14, 2020 |
| MBP | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | Class II | Orthopedic | Contract manufacturing | Jun 29, 2011 |
| MQV | Filler, Bone Void, Calcium Compound | Class II | Orthopedic | Contract manufacturing | Jun 29, 2011 |
| OWW | Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon | Class II | General and plastic surgery | Contract manufacturing | Dec 19, 2017 |