Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / India
FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in India: 5 establishments
5 establishments in India are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 2 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
- India
Makers of Electrosurgical, Cutting & Coagulation & Accessories in India
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medico Electrodes International Ltd | NOIDA Uttar Pradesh, India | Contract manufacturer, Manufacturer | 2 | January 30, 1996 | 0 | 0 | 0 | api.fda.gov |
| Ace Medical Devices Pvt. Ltd | PUNE Maharashtra, India | Specification developer | 1 | July 11, 2016 | 0 | 0 | 0 | api.fda.gov |
| Kaynes Technology India Limited | Mysore Karnataka, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mysore Wifiltronics Pvt. Ltd | Mysore Karnataka, India | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Syrma Johari MedTech Limited | Jodhpur Rajasthan, India | 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.