Data / Medical devices / Massager, Powered Inflatable Tube / South Korea
FDA-registered makers of Massager, Powered Inflatable Tube in South Korea: 5 establishments
5 establishments in South Korea are registered with the FDA to make Massager, Powered Inflatable Tube (product code IRP). 3 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
- Massager, Powered Inflatable Tube
- Product code
- IRP
- Country
- South Korea
Makers of Massager, Powered Inflatable Tube in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Maxstar Industrial Co Ltd | Gimpo Gyeonggi, South Korea | Manufacturer | 5 | September 2, 2021 | 0 | 0 | 0 | api.fda.gov |
| Daesung Maref Co.,ltd | Anyang-si Gyeonggi, South Korea | Manufacturer | 4 | July 19, 2023 | 0 | 0 | 0 | api.fda.gov |
| Daesung Maref Co.,ltd | Gunpo-si Gyeonggi, South Korea | Manufacturer, Specification developer | 4 | July 19, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ceragem Co., Ltd. | Cheonan-si, Seobuk-gu Chungnam, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nuga Medical Co Ltd | Wonju Gangwon, 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.