Data / Medical devices / India / Medico Electrodes International Ltd
Medico Electrodes International Ltd: FDA-registered device maker in NOIDA Uttar Pradesh, India, 3 510(k) clearances
Medico Electrodes International Ltd is registered with the FDA (registration 3004903538) in NOIDA Uttar Pradesh, India. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 30, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004903538
- Address
- Plot 142a/11, 12, 27, 28 & 29 Noida Special Economic Zone, NOIDA Uttar Pradesh, India, 201305
- Owner or operator
- MEDICO ELECTRODES INTERNATIONAL LTD (9064498)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 29, 2012
- Registered through
- 2026
- Brand names listed
- Medico Electrodes, bluESU
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Manufacturer | accessdata.fda.gov |
| Electrode, Electrocardiograph | DRX | 2 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 30, 2016 | K161282 | FlexStim Neurostimulation Electrodes Model Numbers: 5050ROC1S, 5050ROC1W, 5050ROC2S, 5050ROC2W, 5050SQC1S, 5050SQC1W, 5050SQC2S, 5050SQC2W | GXY | Substantially Equivalent | Medico Electrodes International , Ltd. | accessdata.fda.gov |
| January 30, 1996 | K955261 | NEUTRALECT ADULT STANDARD, RETURN (REM) & PAEDIATRIC ELECTROSURGERY PLATE (MODIFICATION) | GEI | Substantially Equivalent | Msb , Ltd. | accessdata.fda.gov |
| November 9, 1994 | K944817 | NEUTRALECT ADULT STANDARD, RETURN (REM), PAEDIATRIC STANDARD, RETURN (REM) | GEI | Substantially Equivalent | Msb , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Electrode, Electrocardiograph
- All makers of Electrode, Cutaneous
Updated October 30, 2016. 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.