Data / Medical devices / Lift, Patient, Non-Ac-Powered / United Kingdom
FDA-registered makers of Lift, Patient, Non-Ac-Powered in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Lift, Patient, Non-Ac-Powered (product code FSA). 0 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
- Lift, Patient, Non-Ac-Powered
- Product code
- FSA
- Country
- United Kingdom
Makers of Lift, Patient, Non-Ac-Powered in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bespoke Stairlifts | Huddersfield Kirklees, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Direct Healthcare Group Limited (THE KIRTON HEALTHCARE GROUP LTD) | Caerphilly, United Kingdom | Manufacturer | 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 | |
| Mangar International Limited | Presteigne Powys, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prism Medical Uk | Rhyl Denbighshire, United Kingdom | Complaint file establishment, 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.