A non-sterile implantable device designed to replace most or all of a dysfunctional intervertebral disc in the cervical spine. It is made of synthetic polymer material(s) [e.g., polyetheretherketone (PEEK)] and typically has a two-plate design, one plate attac
| Company | Devices | Share |
|---|---|---|
| Spinal Elements | 82 | 100% |
Company = labeler of record on GUDID. 1 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 |
|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | 157 |
| MJO | PROSTHESIS, INTERVERTEBRAL DISC | 1 |
Use these as the dimensions to specify in a tender line.
82 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cervical total disc replacement prosthesis, non-sterile", from 1 companies. The largest labeler is Spinal Elements with 100% of records.
KWQ (Appliance, Fixation, Spinal Intervertebral Body), MJO (PROSTHESIS, INTERVERTEBRAL DISC)
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.