Data / Medical devices / Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis) / South Korea
FDA-registered makers of Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis) in South Korea: 10 establishments
10 establishments in South Korea are registered with the FDA to make Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis) (product code JRS). 0 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
- Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis)
- Product code
- JRS
- Country
- South Korea
Makers of Purifier, Water (Absorption, Deionization, Membrane Filter, Reverse Osmosis) in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Biontech Life Co., Ltd | Gunpo-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| D&D Electronics Co., Ltd. | Anyang-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentozone Corporation | Guro-gu Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hanumul Co., Ltd. | Goyang-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hue Light Co., Ltd | Gwangmyeong-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kyk Co.,ltd | Seongnam-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Para Membranes Co., Ltd. | Hwaseong-Si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prime Water Co.,ltd. | Bucheon-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synopex Biofilter | Hwaseong-si Gyeonggi, South Korea | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tae Young E&t Co.,ltd | Yangsan Gyeongnam, 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.