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Data / Medical devices / Drill, Dental, Intraoral / South Korea

FDA-registered makers of Drill, Dental, Intraoral in South Korea: 30 establishments

30 establishments in South Korea are registered with the FDA to make Drill, Dental, Intraoral (product code DZA). 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
Drill, Dental, Intraoral
Product code
DZA
Country
South Korea

Makers of Drill, Dental, Intraoral in South Korea

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
ACH Medical Co., Ltd.Hwaseong-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
ARUM DENTISTRY Co., Ltd.Yuseong-gu Daejeon, South KoreaManufacturer0000api.fda.gov
Biotem Co., Ltd.Busan, South KoreaManufacturer0000api.fda.gov
Cowellmedi Co., Ltd.Busan, South KoreaManufacturer0000api.fda.gov
Cybermed Inc.Daejeon, South KoreaManufacturer0000api.fda.gov
Diadent Group InternationalCHONGJU CITY Chungbuk, South KoreaManufacturer0000api.fda.gov
DIMPLO Ltd.Yeonje-gu Busan, South KoreaManufacturer0000api.fda.gov
DIO CorporationHaeundae-gu Busan, South KoreaManufacturer0000api.fda.gov
Doiff Co., Ltd.Suncheon-si, Jeollanam-do Jeonnam, South KoreaManufacturer0000api.fda.gov
Dunamis Dental Co., Ltd.Gwangmyeong-si Gyeonggi, South KoreaExporter to the US, Manufacturer0000api.fda.gov
Hans KoreaPaju-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Innobiosurg Co., Ltd.Daejeon, South KoreaManufacturer0000api.fda.gov
Izenimplant Co., Ltd.Hwaseong-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Izenimplant Co., Ltd.Pyeongtaek-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Kaiser Precision Co.Hwaseong Gyeonggi, South KoreaManufacturer0000api.fda.gov
MctbioYongin-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Medimecca Co LtdSeoul, South KoreaManufacturer0000api.fda.gov
MegaGen Implant Co., Ltd. (Research Laboratories)Daegu, South KoreaSpecification developer0000api.fda.gov
Megagen Implant Co., Ltd.Daegu, South KoreaManufacturer0000api.fda.gov
Neobiotech Co., Ltd.Wonju-si Gangwon, South KoreaManufacturer0000api.fda.gov
Osstem Implant Co., Ltd.Gangseo-gu Seoul, South KoreaSpecification developer0000api.fda.gov
Osstem Implant Co., Ltd.Haeundae-gu Busan, South KoreaManufacturer0000api.fda.gov
Ossvis Co., Ltd.Anyang-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Osung MND Co., Ltd.Gimpo-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
POINTIMPLANT Co., LtdBusan, South KoreaComplaint file establishment, Manufacturer0000api.fda.gov
Sewon Medix, Inc.Busan, South KoreaManufacturer0000api.fda.gov
Snucone Co., Ltd.Dalseo-gu Daegu, South KoreaManufacturer0000api.fda.gov
Shinhung MST Co., Ltd.Wonju Si Gangwon, South KoreaManufacturer0000api.fda.gov
TruAbutment Korea Co., Ltd.Bucheon-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
WARANTEC Co., Ltd.Seongnam-si 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.