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 |
|---|---|---|
| Ctl Medical Corporation | 626 | 87% |
| Met 1 Technologies, Llc | 95 | 13% |
Company = labeler of record on GUDID. 2 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 | 1,155 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 893 |
| MQP | Spinal Vertebral Body Replacement Device | 120 |
Use these as the dimensions to specify in a tender line.
721 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Ceramic spinal interbody fusion cage", from 2 companies. The largest labeler is Ctl Medical Corporation with 87% of records.
MAX (Intervertebral Fusion Device With Bone Graft, Lumbar), ODP (Intervertebral Fusion Device With Bone Graft, Cervical), MQP (Spinal Vertebral Body Replacement Device)
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.