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Medical Device Contract Manufacturers

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158 profiles

Alphabetical ยท 2 / 14
TOCHIGI, Japan

B. BRAUN AESCULAP JAPAN CO., LTD.

Qualified source record ยท not independently verified

B. BRAUN AESCULAP JAPAN CO., LTD. is listed in FDA device registration data in TOCHIGI, JP with the establishment role โ€œManufacture Medical Device for Another Party (Contract Manufacturer).โ€ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.

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SUNTO-GUN Shizuoka, Japan

Beckman Coulter Mishima K.K.

Qualified source record ยท not independently verified

Beckman Coulter Mishima K.K. is listed in FDA device registration data in SUNTO-GUN Shizuoka, JP with the establishment role โ€œManufacture Medical Device for Another Party (Contract Manufacturer).โ€ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.

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Yawata Ky?to, Japan

BELMONT TECHNO KYOTO CORPORATION

Qualified source record ยท not independently verified

BELMONT TECHNO KYOTO CORPORATION is listed in FDA device registration data in Yawata Ky?to, JP with the establishment role โ€œManufacture Medical Device for Another Party (Contract Manufacturer).โ€ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.

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SUNTO-GUN Shizuoka, Japan

Canon Medical Diagnostics Corporation Fuji Plant.

Qualified source record ยท not independently verified

Canon Medical Diagnostics Corporation Fuji Plant. is listed in FDA device registration data in SUNTO-GUN Shizuoka, JP with the establishment role โ€œManufacture Medical Device for Another Party (Contract Manufacturer).โ€ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.

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Kitakata Fukushima, Japan

COHEN INDUSTRY CO., LTD.

Qualified source record ยท not independently verified

COHEN INDUSTRY CO., LTD. is listed in FDA device registration data in Kitakata Fukushima, JP with the establishment role โ€œManufacture Medical Device for Another Party (Contract Manufacturer).โ€ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.

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Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers

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