Contract manufacturerOAKTREE ADDITIVE (Tampa, FL)FloridaOrthopedicClass II
OAKTREE ADDITIVE
Contract manufacturer ยท Tampa, FL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3023189283 (openFDA record; or search FDA's registration database)
- FEI number
- 3023189283
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- OakTree Additive (FDA owner/operator no. 10085440)
- Registered address
- 14500 McCormick, Tampa, FL 33626
- Contract listings
- 3 device listings, 4 product codes, first listed Jun 17, 2022
- 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 |
|---|---|---|---|---|---|
| HWC | Screw, Fixation, Bone | Class II | Orthopedic | Contract manufacturing | Mar 3, 2026 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | Class II | Orthopedic | Contract manufacturing | Jun 17, 2022 |
| OUR | Sacroiliac Joint Fixation | Class II | Orthopedic | Contract manufacturing | Mar 3, 2026 |
| OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical | Class II | Orthopedic | Contract manufacturing | Mar 3, 2026 |