A sterile implantable artificial substitute for a diseased (e.g., arthritic) or injured hip joint consisting of matching femoral (head/shaft) and acetabular components articulated at a ceramic-on-polyethylene or cross-linked polyethylene (PE) interface. Fixati
| Company | Devices | Share |
|---|---|---|
| United Orthopedic Corp. | 223 | 55% |
| Cpm Medical Consultants, Llc | 52 | 13% |
| Endotec, Inc. | 27 | 7% |
| Kyocera Medical Corporation | 24 | 6% |
| Kyocera Corporation | 24 | 6% |
| Synovo Production | 21 | 5% |
| Conformis, Inc. | 21 | 5% |
| Modal Manufacturing Llc | 11 | 3% |
| Biopro, Inc. | 5 | 1% |
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 |
|---|---|---|
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce | 339 |
| MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polym | 237 |
| LWJ | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented | 221 |
| KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or | 214 |
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | 180 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc | 147 |
Use these as the dimensions to specify in a tender line.
408 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Ceramic-on-polyethylene total hip prosthesis", from 9 companies. The largest labeler is United Orthopedic Corp. with 55% of records.
LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce), MEH (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polym), LWJ (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented), KWY (Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or )
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.