Qualified source record ยท not independently verified
CHEMICHL AG is listed in FDA device registration data in Vaduz, LI with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
ESTETIC CERAM AG is listed in FDA device registration data in Triesen, LI with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
FMA MECHATRONIC SOLUTIONS AG is listed in FDA device registration data in Schaan, LI with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
IVOCLAR VIVADENT AG is listed in FDA device registration data in SCHAAN, LI with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers