TSUBASA INDUSTRY CO., LTD​

In 1988, prior to the enforcement of GMP (Good Manufacturing Practice) for medical devices, in 1955, we acquired the right to bid for the US government and New York City. Since then, I have cleared F.D.A. (U.S. Food & Drug Administration) audits several times.

Currently, we are creating a new system to comply with international standards for quality assurance and quality control.

We always want to provide products of excellent quality and contribute to people's healthy lives. Our reliable technology is born from these feelings for "people”.