A copy of a final transfemoral amputation tissue-reinforcement implant intended to be used during orthopaedic surgery to accurately size a transfemoral amputation tissue-reinforcement implant (medullary canal rod and bulb) prior to implantation, following a tr
| Company | Devices | Share |
|---|---|---|
| Alpha Ai Co.,Ltd. | 110 | 100% |
Company = labeler of record on GUDID. 1 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 |
|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | 78 |
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 32 |
Use these as the dimensions to specify in a tender line.
110 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Transfemoral amputation tissue-reinforcement implant trial", from 1 companies. The largest labeler is Alpha Ai Co.,Ltd. with 100% of records.
LXH (Orthopedic Manual Surgical Instrument), ODP (Intervertebral Fusion Device With Bone Graft, Cervical)
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.