Medical Device Contract Manufacturers
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Qualified source record · not independently verified
KYOCERA Medical Corporation Shiga Yasu Plant is listed in FDA device registration data in Yasu-shi 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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KYOWA, LTD. is listed in FDA device registration data in IZUMISANO-CITY ?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.
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LITM INC. is listed in FDA device registration data in 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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LIVEDO CORPORATION is listed in FDA device registration data in CHUO KU 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.
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MANI, INC. (HANAOKA FACTORY) is listed in FDA device registration data in SHIOYA 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.
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MANI, INC. (HEAD OFFICE) is listed in FDA device registration data in UTSUNOMIYA 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.
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MANI, INC. (TAKANEZAWA FACILITY) is listed in FDA device registration data in SHIOYA 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.
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MARI VISION, INC. is listed in FDA device registration data in ABENO-KU ?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.
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MARUEMU WORKS CO.,LTD. is listed in FDA device registration data in Daitoshi ?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.
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MARVEL 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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MASAHIRO MARUYAMA INC. is listed in FDA device registration data in Shibuya-ku 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
MATSUNAMI GLASS IND.,LTD is listed in FDA device registration data in Kishiwada City ?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 →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