A multiple-strand (multifilament), synthetic thread made from a non-bioabsorbable polyester intended to join (i.e., approximate) the edges of a soft-tissue wound or incision by stitching or to ligate soft tissues; it may include an attached disposable device(s
| Company | Devices | Share |
|---|---|---|
| Teleflex Incorporated | 1,180 | 29% |
| Demetech Corporation | 978 | 24% |
| Ethicon, Llc | 735 | 18% |
| Covidien Lp | 357 | 9% |
| Peters Surgical | 162 | 4% |
| Foosin Medical Supplies Inc., Ltd. | 123 | 3% |
| Surgical Specialties México, S. De R.L. De C.V. | 96 | 2% |
| Internacional Farmacéutica, S.A. De C.V. | 49 | 1% |
| Meril Endo Surgery Private Limited | 47 | 1% |
| C.P. Medical Corporation | 40 | 1% |
| Shandong Haidike Medical Products Co., Ltd. | 39 | 1% |
| Fusion Orthopedics, Llc | 33 | 1% |
Company = labeler of record on GUDID. 42 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 | 4,155 |
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene | 1,412 |
| GAQ | SUTURE, NONABSORBABLE, STEEL, MONOFILAMENT AND MULTIFILAMENT | 339 |
| GAS | Suture, Nonabsorbable, Synthetic, Polyester | 113 |
| GAT | Suture, nonabsorbable, synthetic, polyethylene | 82 |
| MBI | Fastener, fixation, nondegradable, soft tissue | 22 |
Use these as the dimensions to specify in a tender line.
4,063 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial", from 42 companies. The largest labeler is Teleflex Incorporated with 29% of records.
GAT (SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE), GAT (Suture, Nonabsorbable, Synthetic, Polyethylene), GAQ (SUTURE, NONABSORBABLE, STEEL, MONOFILAMENT AND MULTIFILAMENT), GAS (Suture, Nonabsorbable, Synthetic, Polyester)
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.