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Data / Medical devices / Dam, Rubber / South Korea

FDA-registered makers of Dam, Rubber in South Korea: 5 establishments

5 establishments in South Korea are registered with the FDA to make Dam, Rubber (product code EIE). 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
Dam, Rubber
Product code
EIE
Country
South Korea

Makers of Dam, Rubber in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
B&L Biotech Co., IncAnsan City Gyeonggi, South KoreaManufacturer0000api.fda.gov
Hdi Inc.Seongnam-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Mediclus Co., LtdCheongju-si Chungbuk, South KoreaManufacturer0000api.fda.gov
Osung MND Co., Ltd.Gimpo-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Spident Co., Ltd.INCHEON Gyeonggi, 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.