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Data / Medical devices / Crown And Bridge, Temporary, Resin / South Korea

FDA-registered makers of Crown And Bridge, Temporary, Resin in South Korea: 7 establishments

7 establishments in South Korea are registered with the FDA to make Crown And Bridge, Temporary, Resin (product code EBG). 6 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
Crown And Bridge, Temporary, Resin
Product code
EBG
Country
South Korea

Makers of Crown And Bridge, Temporary, Resin in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Diadent Group InternationalCHONGJU CITY Chungbuk, South KoreaManufacturer2February 13, 2020000api.fda.gov
Meta Biomed Co., Ltd.Cheongju-si Chungbuk, South KoreaManufacturer2July 3, 2019000api.fda.gov
ARUM DENTISTRY Co., Ltd.Yuseong-gu Daejeon, South KoreaManufacturer1December 8, 2021000api.fda.gov
Dentis Co., Ltd.Daegu, South KoreaManufacturer1December 7, 2018000api.fda.gov
Mgnewton Ltd.Gyengsan-si Gyeongbuk, South KoreaManufacturer1December 21, 2022000api.fda.gov
Spident Co., Ltd.INCHEON Gyeonggi, South KoreaManufacturer1March 10, 2022000api.fda.gov
Graphy Inc.Seoul, South KoreaExporter to the US, 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.