Data / Medical devices / Stimulator, Muscle, Powered / United Kingdom
FDA-registered makers of Stimulator, Muscle, Powered in the United Kingdom: 6 establishments
6 establishments in the United Kingdom are registered with the FDA to make Stimulator, Muscle, Powered (product code IPF). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Stimulator, Muscle, Powered
- Product code
- IPF
- Country
- United Kingdom
Makers of Stimulator, Muscle, Powered in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Firstkind Ltd | High Wycombe Buckinghamshire, United Kingdom | Specification developer | 3 | March 4, 2022 | 0 | 0 | 0 | api.fda.gov |
| Actegy Ltd. | Bracknell, United Kingdom | Specification developer | 1 | June 28, 2013 | 0 | 0 | 0 | api.fda.gov |
| Digitimer Ltd. | Welwyn Garden City Hertfordshire, United Kingdom | Complaint file establishment, Manufacturer | 1 | March 6, 2018 | 0 | 0 | 0 | api.fda.gov |
| Gwalia Healthcare Limited | PONTYPRIDD Wales, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Odstock Medical Ltd | SALISBURY Wiltshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Magstim Company Ltd. | Carmarthenshire Wales, 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.