Data / Medical devices / Hand, External Limb Component, Mechanical / United Kingdom
FDA-registered makers of Hand, External Limb Component, Mechanical in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Hand, External Limb Component, Mechanical (product code IRA). 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
- Hand, External Limb Component, Mechanical
- Product code
- IRA
- Country
- United Kingdom
Makers of Hand, External Limb Component, Mechanical in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hugh Steeper Ltd | Leeds, England, United Kingdom | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Koalaa | London London, City of, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Metacarpal Ltd | Edinburgh Edinburgh, City of, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Open Bionics | Bristol Bristol, City of, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Touch Bionics Ltd | Livingston West Lothian, United Kingdom | Specification developer | 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.