Medical Device Contract Manufacturers
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Qualified source record · not independently verified
HUREV CO., LTD. is listed in FDA device registration data in Gangwon-do, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
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HUVITZ CO., LTD. is listed in FDA device registration data in Anyang-si Gyeonggi, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
HYDROCHEM CO., LTD is listed in FDA device registration data in Gangeung-Si Gangwon, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
INSTITUTE OF ADVANCED CONVERGENCE TECHNOLOGY (IACT) is listed in FDA device registration data in Daegu, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
INTOPS CO.,LTD. is listed in FDA device registration data in Suwon Gyeonggi, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
IRAY KOREA LIMITED is listed in FDA device registration data in Seoul, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
i-SENS Songdo Factory is listed in FDA device registration data in Incheon, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
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I-SENS Songdo Factory 2 is listed in FDA device registration data in lncheon Incheon, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
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i-SENS Wonju Factory is listed in FDA device registration data in Wonju-si Gangwon, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
JINSUNG OPTICAL CO. is listed in FDA device registration data in DAEGU, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
JM TECH, LTD. CO. is listed in FDA device registration data in Incheon, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Qualified source record · not independently verified
KAESUNG CO., LTD. is listed in FDA device registration data in Bucheon-Si Gyeonggi, KR with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Request supplier options →Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers
South Korea