Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / United Kingdom
FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in the United Kingdom: 10 establishments
10 establishments in the United Kingdom are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 6 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
- Electrosurgical, Cutting & Coagulation & Accessories
- Product code
- GEI
- Country
- United Kingdom
Makers of Electrosurgical, Cutting & Coagulation & Accessories in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Morgan Steer Orthopaedics Ltd | Leicester Leicestershire, United Kingdom | Specification developer | 4 | August 22, 2013 | 0 | 0 | 0 | api.fda.gov |
| Energist Limited | Swansea, United Kingdom | Manufacturer | 2 | January 12, 2023 | 0 | 0 | 0 | api.fda.gov |
| Purple Surgical International Limited | Herts England, United Kingdom | Specification developer | 2 | November 21, 2014 | 0 | 0 | 0 | api.fda.gov |
| Surgical Innovations Ltd | Leeds, United Kingdom | Manufacturer | 2 | January 26, 2012 | 0 | 0 | 0 | api.fda.gov |
| Creo Medical Ltd | CHEPSTOW Monmouthshire, United Kingdom | Specification developer | 1 | February 5, 2025 | 0 | 0 | 0 | api.fda.gov |
| Nissha Medical Technologies Limited | Paignton Devon, United Kingdom | Manufacturer | 1 | February 23, 2021 | 0 | 0 | 0 | api.fda.gov |
| Alesi Surgical Ltd | Cardiff, United Kingdom | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cme Devices Ltd | CHEPSTOW Monmouthshire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gyrus Medical Ltd. | CARDIFF Wales, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Purple Surgical Manufacturing Limited | Taunton Somerset, United Kingdom | Contract 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.