Data / Medical devices / Mesh, Surgical, Polymeric / United Kingdom
FDA-registered makers of Mesh, Surgical, Polymeric in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Mesh, Surgical, Polymeric (product code FTL). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Mesh, Surgical, Polymeric
- Product code
- FTL
- Country
- United Kingdom
Makers of Mesh, Surgical, Polymeric in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Xiros Ltd | YEADON Leeds, United Kingdom | Contract manufacturer, Manufacturer | 3 | May 31, 2023 | 0 | 0 | 0 | api.fda.gov |
| Lockdown Medical Limited | Redditch Worcestershire, United Kingdom | Manufacturer | 1 | July 24, 2008 | 0 | 0 | 0 | api.fda.gov |
| Entaco Ltd. | Redditch Worcestershire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew Medical Ltd | HULL East Riding of Yorkshire, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgical Specialties Corporation Limited (UK) | Taunton Somerset, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.