A non-bioabsorbable, implantable device designed to be inserted into the medullary canal of a bone (e.g., femur, tibia, or humerus) during orthopaedic surgery to prevent cement progression in the diaphysis and therefore facilitate cement pressurization during
| Company | Devices | Share |
|---|---|---|
| Howmedica Osteonics Corp. | 61 | 35% |
| Zimmer, Inc. | 24 | 14% |
| Biomet Orthopedics, Llc | 15 | 9% |
| Waldemar Link Gmbh & Co. Kg | 13 | 8% |
| Smith & Nephew, Inc. | 9 | 5% |
| Orthomedflex Llc | 9 | 5% |
| Depuy (Ireland) | 9 | 5% |
| Signature Orthopaedics Pty Ltd | 8 | 5% |
| B-One Ortho, Corp. | 7 | 4% |
| Ortho Development Corporation | 6 | 3% |
| Medacta International Sa | 5 | 3% |
| Tecres Spa | 4 | 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 |
|---|---|---|
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 74 |
| LZN | CEMENT OBTURATOR | 51 |
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or | 35 |
| LWJ | Prosthesis, hip, semi-constrained, metal/polymer, uncemented | 29 |
| MBL | Prosthesis, hip, semi-constrained, uncemented, metal/polymer | 29 |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce | 29 |
Use these as the dimensions to specify in a tender line.
173 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Polymer orthopaedic cement restrictor, non-bioabsorbable", from 13 companies. The largest labeler is Howmedica Osteonics Corp. with 35% of records.
JDI (Prosthesis, hip, semi-constrained, metal/polymer, cemented), LZN (CEMENT OBTURATOR), KWY (Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or ), LWJ (Prosthesis, hip, semi-constrained, metal/polymer, uncemented)
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.