Medical Device Contract Manufacturers
Find a manufacturing partner by capability, industry and company location.
Qualified source record · not independently verified
AirLife Finland Oy is listed in FDA device registration data in Helsinki Uusimaa, FI 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
ARCTIC BIOMATERIALS OY is listed in FDA device registration data in Tampere Pirkanmaa, FI 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
INION OY is listed in FDA device registration data in TAMPERE Pirkanmaa, FI 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
INNOKAS MEDICAL OY is listed in FDA device registration data in KEMPELE Pohjois-Pohjanmaa, FI 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
KB Components Finland Oy is listed in FDA device registration data in Nurmijarvi Etela-Karjala, FI 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
KYTOLA INSTRUMENTS OY is listed in FDA device registration data in Muurame Keski-Suomi, FI 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
LM-INSTRUMENTS OY is listed in FDA device registration data in PARAINEN Varsinais-Suomi, FI 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
MARIACHI OY is listed in FDA device registration data in Littoinen Varsinais-Suomi, FI 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
MECTALENT LTD. is listed in FDA device registration data in Oulu Kainuu, FI 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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MODULIGHT CORPORATION is listed in FDA device registration data in Tampere Pirkanmaa, FI 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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OY PRIMO FINLAND AB is listed in FDA device registration data in Vaasa Pohjanmaa, FI 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
SCREENTEC OY is listed in FDA device registration data in Oulu, Finland Pohjois-Pohjanmaa, FI 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
Finland