A sterile implantable device designed to replace the proximal femoral neck as part of a total hip arthroplasty (THA). The device is contoured to enable fixation by pressing the distal end into the cortex of the remaining natural femur to achieve a mechanical i
| Company | Devices | Share |
|---|---|---|
| Howmedica Osteonics Corp. | 729 | 23% |
| Biomet Orthopedics, Llc | 495 | 16% |
| Smith & Nephew, Inc. | 370 | 12% |
| Exactech, Inc. | 295 | 9% |
| Zimmer, Inc. | 236 | 7% |
| Implantcast Gmbh | 155 | 5% |
| Globus Medical, Inc. | 146 | 5% |
| Limacorporate Spa | 122 | 4% |
| Orthomedflex Llc | 107 | 3% |
| Microport Orthopedics Inc. | 96 | 3% |
| Maxx Orthopedics, Inc. | 93 | 3% |
| B-One Ortho, Corp. | 83 | 3% |
Company = labeler of record on GUDID. 20 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 | 1,627 |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC | 1,431 |
| MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer | 1,245 |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 988 |
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or | 851 |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce | 816 |
Use these as the dimensions to specify in a tender line.
3,165 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Press-fit femoral stem prosthesis", from 20 companies. The largest labeler is Howmedica Osteonics Corp. with 23% of records.
LZO (Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce), LPH (PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC), MEH (Prosthesis, hip, semi-constrained, uncemented, metal/polymer), JDI (Prosthesis, hip, semi-constrained, metal/polymer, cemented)
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.