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Data / Medical devices / System, Isokinetic Testing And Evaluation / South Korea

FDA-registered makers of System, Isokinetic Testing And Evaluation in South Korea: 8 establishments

8 establishments in South Korea are registered with the FDA to make System, Isokinetic Testing And Evaluation (product code IKK). 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
System, Isokinetic Testing And Evaluation
Product code
IKK
Country
South Korea

Makers of System, Isokinetic Testing And Evaluation in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cosmo Robotics Co., LtdSeoul, South KoreaManufacturer0000api.fda.gov
CUREXO, Inc.Songpa-gu Seoul, South KoreaManufacturer0000api.fda.gov
H Robotics Inc.Yeonsu-gu Incheon, South KoreaManufacturer0000api.fda.gov
Hue Light Co., LtdGwangmyeong-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
InBody Co, Ltd.Cheonan-si Chungnam, South KoreaManufacturer0000api.fda.gov
Korea Body InformationSeoul, South KoreaManufacturer0000api.fda.gov
Man & Company LimitedGumi-Si Gyeongbuk, South KoreaManufacturer0000api.fda.gov
P&S Robotics Co.,ltdSeoul, 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.