Medical Device Contract Manufacturers
Find a manufacturing partner by capability, industry and company location.
Qualified source record · not independently verified
Promega Biosystems Inc. 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
RAY 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
REMED Co., Ltd. is listed in FDA device registration data in Cheongju-si Chungbuk, 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
SEWOON MEDICAL CO., LTD. is listed in FDA device registration data in Cheonan-si Chungnam, 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
SHERPA KOREA is listed in FDA device registration data in Saha-gu Busan, 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
SHINA CORP. is listed in FDA device registration data in GONGJU-SI Chungnam, 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
SHINA MED CORPORATION 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
Siemens Healthineers Ltd. is listed in FDA device registration data in Pohang-si Gyeongbuk, 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
SKIDYWORKS INTERNATIONAL CO., LTD is listed in FDA device registration data in JEJU, 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
SMD DENTAL LABORATORY is listed in FDA device registration data in Heungdeok-gu Cheongju-si Chungbuk, 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
SMILELAB CO., LTD. is listed in FDA device registration data in Seongnam-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
SML GENETREE CO. LTD. 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