A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease
| Company | Devices | Share |
|---|---|---|
| Nuvasive, Inc. | 7,488 | 11% |
| Alphatec Spine, Inc. | 6,222 | 9% |
| Globus Medical, Inc. | 4,595 | 7% |
| Orthofix Us Llc | 4,299 | 6% |
| Gbs Commonwealth Co.,Ltd. | 3,938 | 6% |
| Degen Medical, Inc. | 2,800 | 4% |
| Medacta International Sa | 2,348 | 3% |
| Gs Medical Co., Ltd. | 2,182 | 3% |
| Medtronic Sofamor Danek, Inc. | 2,077 | 3% |
| Astura Medical | 2,031 | 3% |
| Nexxt Spine, Llc | 1,867 | 3% |
| L&K Biomed Co. ,Ltd. | 1,825 | 3% |
Company = labeler of record on GUDID. 107 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 | 30,012 |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 23,973 |
| PHM | Intervertebral fusion device with bone graft, thoracic | 13,531 |
| OVD | Intervertebral fusion device with integrated fixation, lumba | 12,611 |
| ODP | Intervertebral fusion device with bone graft, cervical | 8,387 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 5,206 |
Use these as the dimensions to specify in a tender line.
69,611 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Metallic spinal interbody fusion cage", from 107 companies. The largest labeler is Nuvasive, Inc. with 11% of records.
MAX (Intervertebral fusion device with bone graft, lumbar), MAX (Intervertebral Fusion Device With Bone Graft, Lumbar), PHM (Intervertebral fusion device with bone graft, thoracic), OVD (Intervertebral fusion device with integrated fixation, lumba)
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.