Skip to the page

Data / Medical devices / Resin, Root Canal Filling / South Korea

FDA-registered makers of Resin, Root Canal Filling in South Korea: 8 establishments

8 establishments in South Korea are registered with the FDA to make Resin, Root Canal Filling (product code KIF). 8 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
Resin, Root Canal Filling
Product code
KIF
Country
South Korea

Makers of Resin, Root Canal Filling in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Meta Biomed Co., Ltd.Cheongju-si Chungbuk, South KoreaManufacturer8September 29, 2023000api.fda.gov
Diadent Group InternationalCHONGJU CITY Chungbuk, South KoreaManufacturer5March 25, 2021000api.fda.gov
MaruchiWonju-si Gangwon, South KoreaManufacturer4February 14, 2023000api.fda.gov
Mediclus Co., LtdCheongju-si Chungbuk, South KoreaManufacturer4January 12, 2026000api.fda.gov
Vericom Co., Ltd.Chuncheon-Si Gangwon, South KoreaManufacturer4September 19, 2025000api.fda.gov
BioMTADaejeon, South KoreaManufacturer2April 10, 2014000api.fda.gov
Spident Co., Ltd.INCHEON Gyeonggi, South KoreaManufacturer2September 11, 2026000api.fda.gov
GENOSS Co., Ltd.Suwon-si Gyeonggi, South KoreaManufacturer1July 28, 2023000api.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.