Medical Device Contract Manufacturers
Find a manufacturing partner by capability, industry and company location.
Qualified source record · not independently verified
KINGTOPS CO., LTD. is listed in FDA device registration data in Gwangyang-si, Jeollanam-do Jeonbuk, 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
KJ MEDITECH CO., LTD. is listed in FDA device registration data in Gwangju, 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
KM HEALTHCARE is listed in FDA device registration data in Cheorwon-gun, 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.
Request supplier options →Qualified source record · not independently verified
Korea First R&D 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
KUSNOW is listed in FDA device registration data in Yongin 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
LABNPEOPLE is listed in FDA device registration data in Yangju-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
L&K BIOMED CO.,LTD. is listed in FDA device registration data in Yongin-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
LUCKY INDUSTRIES CO., LTD. is listed in FDA device registration data in Gwangju Jeonnam, 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
MEDEXEL CO., LTD. is listed in FDA device registration data in Anseong-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
MEDIANA CO., LTD. is listed in FDA device registration data in Wonju-Si, 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.
Request supplier options →Qualified source record · not independently verified
MEDIKAN CO., Ltd. is listed in FDA device registration data in Gangseo-gu 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
MEDIT CORP. 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 →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