Data / Medical devices / Electrode, Electrocardiograph / South Korea
FDA-registered makers of Electrode, Electrocardiograph in South Korea: 5 establishments
5 establishments in South Korea are registered with the FDA to make Electrode, Electrocardiograph (product code DRX). 1 has 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
- Electrode, Electrocardiograph
- Product code
- DRX
- Country
- South Korea
Makers of Electrode, Electrocardiograph in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bio Protech, Inc. | Wonju-si Gangwon, South Korea | Manufacturer | 4 | November 7, 2008 | 0 | 0 | 0 | api.fda.gov |
| Dreamtech Co., Ltd. | Asan-si Chungnam, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Daehan Medical Systems Co., Ltd. Commerce | Incheon, South Korea | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hurev Co., Ltd. | Gangwon-do, South Korea | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| InBody Co, Ltd. | Cheonan-si Chungnam, South Korea | 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.