Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / Canada
FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in Canada: 8 establishments
8 establishments in Canada are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 7 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
- Canada
Makers of Electrosurgical, Cutting & Coagulation & Accessories in Canada
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Inbella Medical Inc. | Richmond Hill Ontario, Canada | Manufacturer | 5 | January 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| Solventum Canada Limited | Morden Manitoba, Canada | Manufacturer | 5 | February 3, 1998 | 0 | 0 | 0 | api.fda.gov |
| Baylis Medical Technologies Inc. | Mississauga Ontario, Canada | Complaint file establishment, Contract manufacturer, Manufacturer | 2 | August 30, 2013 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Mississauga Ontario, Canada | Manufacturer, Specification developer | 2 | November 7, 2012 | 0 | 0 | 0 | api.fda.gov |
| Jac-Cell Medic | Mont - Royal Quebec, Canada | Manufacturer | 1 | February 28, 2017 | 0 | 0 | 0 | api.fda.gov |
| Orbsurgical Ltd. | Calgary Alberta, Canada | Manufacturer | 1 | July 29, 2005 | 0 | 0 | 0 | api.fda.gov |
| Walsh Medical Devices, Inc. | OAKVILLE Ontario, Canada | Manufacturer | 1 | July 17, 2003 | 0 | 0 | 0 | api.fda.gov |
| Luvo Medical Technologies, Inc. | Cambridge Ontario, Canada | 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.