A copy of a final femoral head prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size, and to help achieve the desired offset, leg-length, and range of motion of the final prosthesis to be implanted. It is one of
| Company | Devices | Share |
|---|---|---|
| Biomet Orthopedics, Llc | 607 | 19% |
| Howmedica Osteonics Corp. | 359 | 11% |
| Smith & Nephew, Inc. | 349 | 11% |
| Zimmer, Inc. | 292 | 9% |
| United Orthopedic Corp. | 189 | 6% |
| Corin Ltd | 180 | 6% |
| Ortho Development Corporation | 166 | 5% |
| Depuy (Ireland) | 150 | 5% |
| Exactech, Inc. | 105 | 3% |
| Waldemar Link Gmbh & Co. Kg | 96 | 3% |
| Biomet Uk Ltd | 91 | 3% |
| Total Joint Orthopedics, Inc. | 76 | 2% |
Company = labeler of record on GUDID. 32 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 |
|---|---|---|
| HWT | TEMPLATE | 1,130 |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 500 |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC | 497 |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce | 494 |
| KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/ | 363 |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 361 |
Use these as the dimensions to specify in a tender line.
3,237 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Femoral head prosthesis trial", from 32 companies. The largest labeler is Biomet Orthopedics, Llc with 19% of records.
HWT (TEMPLATE), JDI (Prosthesis, hip, semi-constrained, metal/polymer, cemented), LPH (PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC), LZO (Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce)
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.