An implantable, prefabricated component of a total shoulder prosthesis (glenoid component) designed to replace or repair the glenoid fossa; it is not a custom-made device. It is cup-like in shape and typically made of polyethylene (PE), but may be made of meta
| Company | Devices | Share |
|---|---|---|
| Limacorporate Spa | 227 | 25% |
| Zimmer, Inc. | 121 | 13% |
| Depuy Orthopaedics, Inc. | 77 | 8% |
| Smith & Nephew, Inc. | 70 | 8% |
| Biomet Orthopedics, Llc | 64 | 7% |
| Tornier | 63 | 7% |
| Arthrex, Inc. | 63 | 7% |
| Exactech, Inc. | 44 | 5% |
| Fx Solutions | 42 | 5% |
| Shoulder Innovations, Inc. | 34 | 4% |
| Tornier, Inc. | 24 | 3% |
| Catalyst Orthoscience Inc. | 15 | 2% |
Company = labeler of record on GUDID. 19 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 |
|---|---|---|
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENT | 555 |
| KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cement | 298 |
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTE | 270 |
| KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemente | 247 |
| PHX | Shoulder Prosthesis, Reverse Configuration | 237 |
| HSD | PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED | 224 |
Use these as the dimensions to specify in a tender line.
910 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Shoulder glenoid fossa prosthesis, prefabricated", from 19 companies. The largest labeler is Limacorporate Spa with 25% of records.
KWS (PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENT), KWS (Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cement), KWT (PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTE), 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.