Medical Device Contract Manufacturers
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Qualified source record · not independently verified
MD INSTRUMENTS MFG. CO.,LTD. is listed in FDA device registration data in Inashiki-Gun Ibaraki, JP 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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MEDICATEC INC. is listed in FDA device registration data in Yashio-shi Saitama, JP 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
MEDMETALEX CO., LTD. is listed in FDA device registration data in Osaka ?saka, JP 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
MITAKA KOHKI CO., LTD. is listed in FDA device registration data in MITAKA SHI T?ky?, JP 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
MORITA ELECTRIC MFG., LTD. is listed in FDA device registration data in HIKONE Shiga, JP 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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NAKANISHI INC. is listed in FDA device registration data in Kanuma Tochigi, JP 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
Nanbu Plastics Co., Ltd. Fujieda Factory is listed in FDA device registration data in Fujieda-shi Shizuoka, JP 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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NASKA CO., LTD. is listed in FDA device registration data in Yokohama Kanagawa, JP 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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NEXUS, INC. is listed in FDA device registration data in Sabae Fukui, JP 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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NIHON CHUSHASHIN KOGYO CO. LTD. is listed in FDA device registration data in Koga Ibaraki, JP 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
NIHON DEMPA KOGYO CO., LTD. is listed in FDA device registration data in Sayama-shi Saitama, JP 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
NIHON SEIMITSU SOKKI CO., LTD. is listed in FDA device registration data in SHIBUKAWA Gunma, JP 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
Japan