A sterile implantable device designed to replace the patellofemoral articulating surface of the knee to treat isolated patellofemoral disease, typically osteoarthritis. The device is made of metal (e.g., oxidized zirconium alloy) and is not coated with a mater
| Company | Devices | Share |
|---|---|---|
| Biomet Orthopedics, Llc | 59 | 38% |
| Medacta International Sa | 24 | 15% |
| Biomet Sports Medicine, Llc | 21 | 13% |
| Mako Surgical Corp. | 16 | 10% |
| Zimmer, Inc. | 10 | 6% |
| Corin Ltd | 9 | 6% |
| Smith & Nephew, Inc. | 8 | 5% |
| Episurf Operations Ab | 6 | 4% |
| Kinamed, Inc. | 4 | 3% |
Company = labeler of record on GUDID. 9 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 |
|---|---|---|
| KRR | PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTE | 136 |
| HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, M | 24 |
| HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, | 18 |
| KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemente | 18 |
| NPJ | PROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAI | 16 |
| HSX | Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, M | 12 |
Use these as the dimensions to specify in a tender line.
157 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Patellofemoral joint prosthesis", from 9 companies. The largest labeler is Biomet Orthopedics, Llc with 38% of records.
KRR (PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTE), HSX (PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, M), HRY (PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, ), KRR (Prosthesis, Knee, Patello/Femoral, Semi-Constrained, 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.