A sterile implantable device typically designed to be attached to a revision femoral stem prosthesis, knee femur prosthesis, femur/tibia shaft prosthesis, or body femoral/tibial extension stem to extend length to compensate for bone loss during revision arthro
| Company | Devices | Share |
|---|---|---|
| Adler Ortho Spa | 34 | 61% |
| Smith & Nephew, Inc. | 9 | 16% |
| Implantcast Gmbh | 7 | 12% |
| Waldemar Link Gmbh & Co. Kg | 3 | 5% |
| Biomet Orthopedics, Llc | 1 | 2% |
| Total Joint Orthopedics, Inc. | 1 | 2% |
| Corentec Co., Ltd | 1 | 2% |
Company = labeler of record on GUDID. 7 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 | 44 |
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | 37 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc | 34 |
| MBL | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer | 34 |
| MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer | 10 |
| LWJ | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented | 3 |
Use these as the dimensions to specify in a tender line.
56 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Sleeve femoral/tibial extension, uncoated", from 7 companies. The largest labeler is Adler Ortho Spa with 61% of records.
LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce), JDI (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented), LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc), MBL (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer)
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.