Skip to the page

Data / Medical devices / Pad, Menstrual, Unscented / South Korea

FDA-registered makers of Pad, Menstrual, Unscented in South Korea: 18 establishments

18 establishments in South Korea are registered with the FDA to make Pad, Menstrual, Unscented (product code HHD). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Pad, Menstrual, Unscented
Product code
HHD
Country
South Korea

Makers of Pad, Menstrual, Unscented in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Authentic Brands Korea Co.,ltdMungyeong-si Gyeongbuk, South KoreaManufacturer0000api.fda.gov
Boldy Inc.Donghae-si Gangwon, South KoreaManufacturer0000api.fda.gov
CHL Korea Co. Ltd.Gangnam-gu Seoul, South KoreaManufacturer0000api.fda.gov
Huez Haus Seoul Co., LtdSongpa-gu Seoul, South KoreaManufacturer0000api.fda.gov
Hibetter CO.,LTDSeongdong-gu Seoul, South KoreaManufacturer0000api.fda.gov
Inertia Inc.Daejeon,, South KoreaManufacturer0000api.fda.gov
International Tissue Co., Ltd.Busan, South KoreaSpecification developer0000api.fda.gov
J2lfa Co., Ltd.Songpa-Gu Seoul, South KoreaManufacturer0000api.fda.gov
Kingtops Co., Ltd.Gwangyang-si, Jeollanam-do Jeonbuk, South KoreaContract manufacturer, Manufacturer0000api.fda.gov
KleanNara Co., LtdSeoul, South KoreaComplaint file establishment, Contract sterilizer, Manufacturer, Specification developer0000api.fda.gov
Lemon Co., LtdGumi-si Gyeongbuk, South KoreaManufacturer0000api.fda.gov
Mirae Well Life Co.,ltdNonsan, South KoreaManufacturer0000api.fda.gov
Rimex International Co., Ltd.Suwon-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Seolim.co., LtdChungju-si Chungbuk, South KoreaManufacturer0000api.fda.gov
Shinwoo P&C Co., Ltd.Chilgok Gyeongbuk, South KoreaManufacturer0000api.fda.gov
SSK Co.,LtdEumseong-gun Chungbuk, South KoreaExporter to the US, Manufacturer0000api.fda.gov
Taebong Co.,ltd.Gwangsan-gu Gwangju, South KoreaManufacturer0000api.fda.gov
WELCRON HEALTHCARE Co., Ltd.Bupyeong-gu Incheon, South KoreaManufacturer0000api.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.