A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It
| Company | Devices | Share |
|---|---|---|
| Tyber Medical, Llc | 2,142 | 25% |
| Seaspine Orthopedics Corporation | 2,058 | 24% |
| Alphatec Spine, Inc. | 812 | 9% |
| Spinal Elements, Inc. | 620 | 7% |
| Precision Spine, Inc. | 464 | 5% |
| Nanovis Spine, Llc | 341 | 4% |
| Xtant Medical Holdings, Inc. | 284 | 3% |
| Nuvasive, Inc. | 196 | 2% |
| Degen Medical, Inc. | 195 | 2% |
| Orthofix Us Llc | 171 | 2% |
| Silony Medical Gmbh | 164 | 2% |
| Medtronic Sofamor Danek, Inc. | 160 | 2% |
Company = labeler of record on GUDID. 28 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| MAX | Intervertebral fusion device with bone graft, lumbar | 4,077 |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2,392 |
| OVD | Intervertebral fusion device with integrated fixation, lumba | 1,608 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 1,550 |
| ODP | Intervertebral fusion device with bone graft, cervical | 1,202 |
| PHM | Intervertebral fusion device with bone graft, thoracic | 1,061 |
Use these as the dimensions to specify in a tender line.
8,648 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Metal-polymer composite spinal interbody fusion cage", from 28 companies. The largest labeler is Tyber Medical, Llc with 25% of records.
MAX (Intervertebral fusion device with bone graft, lumbar), MAX (Intervertebral Fusion Device With Bone Graft, Lumbar), OVD (Intervertebral fusion device with integrated fixation, lumba), ODP (Intervertebral Fusion Device With Bone Graft, Cervical)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.