An assembly of implantable devices designed to treat a patient with complex chest wall and/or spinal deformities, typically thoracic insufficiency syndrome (TIS) in paediatric patients (a congenital condition where severe deformities of the chest, spine, and r
| Company | Devices | Share |
|---|---|---|
| Synthes Gmbh | 172 | 80% |
| Orthopediatrics Corp. | 42 | 20% |
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 |
|---|---|---|
| MDI | Prosthesis, rib replacement | 208 |
| HTD | FORCEPS | 3 |
| KIK | HOOK, BONE | 2 |
| FSM | TRAY, SURGICAL, INSTRUMENT | 1 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
214 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vertical expandable prosthetic rib system", from 2 companies. The largest labeler is Synthes Gmbh with 80% of records.
MDI (Prosthesis, rib replacement), HTD (FORCEPS), KIK (HOOK, BONE), FSM (TRAY, SURGICAL, INSTRUMENT)
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.