Processed (e.g., sterilised, aseptically processed) tendon tissue, harvested from a human donor, which may include a bone block, intended for transplantation to replace or strengthen damaged tendon. It may include non-tissue components (e.g. suture) to facilit
| Company | Devices | Share |
|---|---|---|
| Lifenet Health | 735 | 97% |
| Allosource | 13 | 2% |
| Joint Restoration Foundation Inc | 10 | 1% |
| Rti Surgical, Inc. | 2 | 0% |
| Musculoskeletal Transplant Foundation, Inc. | 1 | 0% |
Company = labeler of record on GUDID. 5 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 |
|---|---|---|
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene | 1,016 |
| GAT | Suture, nonabsorbable, synthetic, polyethylene | 2 |
Use these as the dimensions to specify in a tender line.
761 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tendon graft", from 5 companies. The largest labeler is Lifenet Health with 97% of records.
GAT (Suture, Nonabsorbable, Synthetic, Polyethylene), GAT (Suture, nonabsorbable, synthetic, polyethylene)
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.