A sterile implantable principal component of a total hip prosthesis (acetabular component) designed to replace or repair the acetabulum. The component is of a one-piece construction and is made entirely of metal [e.g., stainless steel, titanium (Ti)]. Devices
| Company | Devices | Share |
|---|---|---|
| Microport Orthopedics Inc. | 235 | 36% |
| B-One Ortho, Corp. | 73 | 11% |
| Corentec Co., Ltd | 70 | 11% |
| Limacorporate Spa | 63 | 10% |
| Novosource, Llc | 40 | 6% |
| Medacta International Sa | 38 | 6% |
| Zimmer, Inc. | 34 | 5% |
| Zimmer Trabecular Metal Technology Inc. | 32 | 5% |
| Howmedica Osteonics Corp. | 18 | 3% |
| Biomet Orthopedics, Llc | 12 | 2% |
| Depuy (Ireland) | 12 | 2% |
| Total Joint Orthopedics, Inc. | 11 | 2% |
Company = labeler of record on GUDID. 13 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 |
|---|---|---|
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc | 274 |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC | 206 |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce | 175 |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce | 105 |
| MBL | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer | 81 |
| MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polym | 74 |
Use these as the dimensions to specify in a tender line.
648 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Metallic acetabulum prosthesis", from 13 companies. The largest labeler is Microport Orthopedics Inc. with 36% of records.
LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc), LPH (PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC), LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce), 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.