Medical Device Contract Manufacturers
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Qualified source record · not independently verified
IKETANI Co., Ltd. is listed in FDA device registration data in Kiso-gun, Nagano-KEN, 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
J. MORITA MFG. CORP. is listed in FDA device registration data in FUSHIMI-KU Ky?to, 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
Kaigen Pharma Co., Ltd. Tenjin Factory is listed in FDA device registration data in Otaru-shi Hokkaid?, 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
KAINOS LABORATORIES, INC., KASAMA FACTORY is listed in FDA device registration data in Kasama 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
KETAKA ELECTRIC Co.,Ltd. is listed in FDA device registration data in Tottori, 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
Kikuyo Factory is listed in FDA device registration data in Kumamoto, 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
KINJO RUBBER CO., LTD. is listed in FDA device registration data in Yao-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 →Qualified source record · not independently verified
Kiyou Jochugiku is listed in FDA device registration data in Kainan Wakayama, 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
KONICA MINOLTA TECHNOPRODUCTS 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
KSI CO., LTD. is listed in FDA device registration data in Gotemba 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.
Request supplier options →Qualified source record · not independently verified
KT TAMASEIKI CO., LTD. is listed in FDA device registration data in Hachiouji 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
KYOCERA Medical Corporation Shiga Higashiomi Plant is listed in FDA device registration data in Higashiomi-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.
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