An implantable artificial substitute for the distal head of the metatarsal or the adjacent phalangeal base, intended to repair an articulating surface of the metatarsophalangeal (MTP) joint of the foot (toe). The device is made of metal or a metal/polymer comb
| Company | Devices | Share |
|---|---|---|
| Biopro, Inc. | 64 | 23% |
| Arthrosurface Incorporated | 49 | 18% |
| Accufix Surgical, Inc. | 40 | 14% |
| Wright Medical Technology, Inc. | 35 | 13% |
| Osteomed Llc | 34 | 12% |
| Biopoly, Llc | 10 | 4% |
| Smith & Nephew, Inc. | 8 | 3% |
| Ascension Orthopedics, Inc. | 8 | 3% |
| Tornier, Inc. | 6 | 2% |
| Nvision Biomedical Technologies, Inc. | 6 | 2% |
| Arthrex, Inc. | 5 | 2% |
| Trilliant Surgical, Llc | 4 | 1% |
Company = labeler of record on GUDID. 15 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 |
|---|---|---|
| KWD | Prosthesis, Toe, Hemi-, Phalangeal | 217 |
| KWD | PROSTHESIS, TOE, HEMI-, PHALANGEAL | 61 |
| LZJ | PROSTHESIS, TOE (METATARSOPHALANGEAL), JOINT, METAL/POLYMER, | 29 |
| LZJ | Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, | 23 |
| HWC | Screw, Fixation, Bone | 6 |
| KWH | PROSTHESIS, TOE, CONSTRAINED, POLYMER | 4 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
276 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Partial metatarsophalangeal joint prosthesis", from 15 companies. The largest labeler is Biopro, Inc. with 23% of records.
KWD (Prosthesis, Toe, Hemi-, Phalangeal), KWD (PROSTHESIS, TOE, HEMI-, PHALANGEAL), LZJ (PROSTHESIS, TOE (METATARSOPHALANGEAL), JOINT, METAL/POLYMER,), LZJ (Prosthesis, Toe (Metatarsophalangeal), Joint, 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.