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Data / Medical devices / Plate, Bone / South Korea

FDA-registered makers of Plate, Bone in South Korea: 9 establishments

9 establishments in South Korea are registered with the FDA to make Plate, Bone (product code JEY). 9 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
Plate, Bone
Product code
JEY
Country
South Korea

Makers of Plate, Bone in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Jeil Medical CorporationSeoul, South KoreaManufacturer7April 2, 2026000api.fda.gov
Jeil Medical CorporationSiheung-si Gyeonggi, South KoreaManufacturer3April 2, 2026000api.fda.gov
Osstem Implant Co., Ltd.Gangseo-gu Seoul, South KoreaSpecification developer3March 26, 2018000api.fda.gov
Osstem Implant Co., Ltd.Haeundae-gu Busan, South KoreaManufacturer3March 26, 2018000api.fda.gov
Osteonic Co., Ltd.Seoul, South KoreaManufacturer2October 20, 2016000api.fda.gov
Biomaterials Korea Inc.Hanam-si Gyeonggi, South KoreaManufacturer1December 8, 2011000api.fda.gov
MegaGen Implant Co., Ltd. (Research Laboratories)Daegu, South KoreaSpecification developer1September 25, 2013000api.fda.gov
Megagen Implant Co., Ltd.Daegu, South KoreaManufacturer1September 25, 2013000api.fda.gov
Surgident Co., Ltd.Dong-gu Daegu, South KoreaManufacturer1May 24, 2018000api.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.