Data / Medical devices / Device, Transfer, Patient, Manual / United Kingdom
FDA-registered makers of Device, Transfer, Patient, Manual in the United Kingdom: 8 establishments
8 establishments in the United Kingdom are registered with the FDA to make Device, Transfer, Patient, Manual (product code FMR). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Device, Transfer, Patient, Manual
- Product code
- FMR
- Country
- United Kingdom
Makers of Device, Transfer, Patient, Manual in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Buckingham Healthcare Ltd | Milborne St Andrew Dorset, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EVAC+CHAIR International Ltd. | Blythe Valley Solihull, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frontier Therapeutics Limited | Tredegar Blaenau Gwent, United Kingdom | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gbuk Group Limited | Selby North Yorkshire, United Kingdom | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Invictus Global Limited | SWADLINCOTE Derbyshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mangar International Limited | Presteigne Powys, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rexyn Ltd | Prescot Liverpool, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thermotraumaport Limited | Ashford Kent, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.