A copy of a final acetabular prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size and position of the final acetabular prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, is typically m
| Company | Devices | Share |
|---|---|---|
| Biomet Orthopedics, Llc | 1,627 | 20% |
| Smith & Nephew, Inc. | 1,370 | 17% |
| Zimmer, Inc. | 1,344 | 16% |
| Depuy (Ireland) | 650 | 8% |
| Howmedica Osteonics Corp. | 559 | 7% |
| United Orthopedic Corp. | 420 | 5% |
| Ortho Development Corporation | 289 | 4% |
| Corentec Co., Ltd | 205 | 2% |
| Exactech, Inc. | 189 | 2% |
| Limacorporate Spa | 181 | 2% |
| Waldemar Link Gmbh & Co. Kg | 160 | 2% |
| Shalby Advanced Technologies, Inc. | 141 | 2% |
Company = labeler of record on GUDID. 34 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 | 2,962 |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC | 1,757 |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 1,701 |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce | 1,616 |
| KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/ | 1,035 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc | 863 |
Use these as the dimensions to specify in a tender line.
8,204 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Acetabulum prosthesis trial, prefabricated, reusable", from 34 companies. The largest labeler is Biomet Orthopedics, Llc with 20% of records.
HWT (TEMPLATE), LPH (PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC), JDI (Prosthesis, hip, semi-constrained, metal/polymer, cemented), 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.