Data / Medical devices / Exerciser, Non-Measuring / United Kingdom
FDA-registered makers of Exerciser, Non-Measuring in the United Kingdom: 11 establishments
11 establishments in the United Kingdom are registered with the FDA to make Exerciser, Non-Measuring (product code ION). 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
- Exerciser, Non-Measuring
- Product code
- ION
- Country
- United Kingdom
Makers of Exerciser, Non-Measuring in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Biometrics Ltd. | Newport Wales, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| C-Pro Direct Ltd | Edenbridge Kent, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cuxson Gerrard & Co., Ltd. | OLDBURY Sandwell, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fireflyfriends Ltd | Lisburn Antrim and Newtownabbey, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Flexicare Medical Ltd. | RHONDDA CYNON TAFF Wales, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Four D Rubber Co Ltd | HEANOR Derbyshire, United Kingdom | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| James Leckey Design Ltd | Lisburn Lisburn and Castlereagh, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meditech Systems Limited | Shaftesbury Dorset, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Owen Mumford Limited | Chipping Norton Oxfordshire, United Kingdom | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Physitrack Plc | London London, City of, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| POWERbreathe International Ltd | SOUTHAM Warwickshire, 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.