Data / Medical devices / Syringe, Piston / United Kingdom
FDA-registered makers of Syringe, Piston in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Syringe, Piston (product code FMF). 4 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
- Syringe, Piston
- Product code
- FMF
- Country
- United Kingdom
Makers of Syringe, Piston in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Owen Mumford Limited | Chipping Norton Oxfordshire, United Kingdom | Complaint file establishment, Contract manufacturer, Foreign private label distributor, Manufacturer, Repackager or relabeler | 2 | December 21, 1998 | 0 | 0 | 0 | api.fda.gov |
| Gbuk Group Limited | Selby North Yorkshire, United Kingdom | Exporter to the US, Specification developer | 1 | November 9, 2017 | 0 | 0 | 0 | api.fda.gov |
| Owen Mumford, Ltd. | Woodstock, Oxfordshire, United Kingdom | Manufacturer | 1 | December 21, 1998 | 0 | 0 | 0 | api.fda.gov |
| Pall Newquay | Newquay Cornwall, United Kingdom | Contract manufacturer, Manufacturer | 1 | September 6, 1994 | 0 | 0 | 0 | api.fda.gov |
| Depuy CMW | Blackpool, Lancashire, United Kingdom | 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.