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Data / Medical devices / Applicator, Absorbent Tipped, Sterile / South Korea

FDA-registered makers of Applicator, Absorbent Tipped, Sterile in South Korea: 9 establishments

9 establishments in South Korea are registered with the FDA to make Applicator, Absorbent Tipped, Sterile (product code KXG). 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
Applicator, Absorbent Tipped, Sterile
Product code
KXG
Country
South Korea

Makers of Applicator, Absorbent Tipped, Sterile in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
BiodyneSeoul, South KoreaManufacturer0000api.fda.gov
HLB Co., Ltd. HealthcareYeondong-myeon Sejong, South KoreaManufacturer0000api.fda.gov
HLB Life Science CO., LTDAnseong-si Gyeonggi, South KoreaContract manufacturer, Manufacturer0000api.fda.gov
Incore Co., Ltd.Daegu, South KoreaManufacturer0000api.fda.gov
PmwcorporationUlsan, South KoreaManufacturer0000api.fda.gov
SG BioScience, INCDongdaemun-gu Seoul, South KoreaManufacturer0000api.fda.gov
Shina Med CorporationAnseong-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Xcell Therapeutics Inc.Yongin-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Yong Chang Co., Ltd.Gimpo Gyeonggi, South KoreaContract manufacturer0000api.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.