A copy of a final internal spinal fixation force sensor, typically mounted on a handle, designed to be used to determine availability of adequate space for the fixation of the final temporary sensor used during the implantation procedure of an internal spinal
| Company | Devices | Share |
|---|---|---|
| Zavation Llc | 861 | 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 |
|---|---|---|
| MQP | Spinal Vertebral Body Replacement Device | 548 |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 271 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 127 |
Use these as the dimensions to specify in a tender line.
861 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Internal spinal fixation force sensor trial", from 1 companies. The largest labeler is Zavation Llc with 100% of records.
MQP (Spinal Vertebral Body Replacement Device), MAX (Intervertebral Fusion Device With Bone Graft, Lumbar), 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.