A sterile implantable device designed to replace the proximal ulna as part of an elbow joint replacement. The device is typically comprised of metal-backed polyethylene (PE) and its stem is usually coated with a material (e.g., porous materials, hydroxyapatite
| Company | Devices | Share |
|---|---|---|
| Encore Medical, L.P. | 46 | 46% |
| Biomet Orthopedics, Llc | 36 | 36% |
| Limacorporate Spa | 17 | 17% |
Company = labeler of record on GUDID. 3 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 |
|---|---|---|
| JDC | PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED | 82 |
| JDB | Prosthesis, Elbow, Semi-Constrained, Cemented | 17 |
| JDC | Prosthesis, Elbow, Constrained, Cemented | 17 |
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTE | 1 |
Use these as the dimensions to specify in a tender line.
99 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Metal-backed elbow ulna prosthesis", from 3 companies. The largest labeler is Encore Medical, L.P. with 46% of records.
JDC (PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED), JDB (Prosthesis, Elbow, Semi-Constrained, Cemented), JDC (Prosthesis, Elbow, Constrained, Cemented), KWT (PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTE)
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.