An implantable device designed to replace one or more vertebral body(s) that has collapsed or been surgically removed due to trauma, tumour or degenerative disease. Also known as a corpectomy or vertebrectomy spacer, it is in the form of a one-piece or modular
| Company | Devices | Share |
|---|---|---|
| Vb Spine Llc | 4,248 | 40% |
| Globus Medical, Inc. | 1,157 | 11% |
| Alphatec Spine, Inc. | 1,156 | 11% |
| Medtronic Sofamor Danek, Inc. | 698 | 7% |
| Nuvasive, Inc. | 595 | 6% |
| Seaspine Orthopedics Corporation | 592 | 6% |
| Biomet Spine Llc | 442 | 4% |
| Synthes Gmbh | 224 | 2% |
| Met 1 Technologies, Llc | 204 | 2% |
| Ulrich Gmbh & Co. Kg | 201 | 2% |
| Zavation Llc | 155 | 1% |
| Next Orthosurgical, Inc. | 130 | 1% |
Company = labeler of record on GUDID. 32 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 |
|---|---|---|
| MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 6,331 |
| MAX | Intervertebral fusion device with bone graft, lumbar | 4,116 |
| ODP | Intervertebral fusion device with bone graft, cervical | 3,074 |
| PLR | Spinal vertebral body replacement device - Cervical | 1,810 |
| MQP | Spinal vertebral body replacement device | 1,549 |
| MQP | Spinal Vertebral Body Replacement Device | 835 |
Use these as the dimensions to specify in a tender line.
10,603 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vertebral body prosthesis", from 32 companies. The largest labeler is Vb Spine Llc with 40% of records.
MQP (SPINAL VERTEBRAL BODY REPLACEMENT DEVICE), MAX (Intervertebral fusion device with bone graft, lumbar), ODP (Intervertebral fusion device with bone graft, cervical), PLR (Spinal vertebral body replacement device - 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.