Toyota Tsusho Corporation is one of 19060 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Toyota Tsusho Corporation - FDA 510(k) Cleared Devices
Recent clearances: UNEXEF-38G ULTRASOUND SYSTEM
1
Total
1
Cleared
0
Denied
Toyota Tsusho Corporation, is a global trading company and member of the Toyota Group. The company operates with a manufacturing facility in San Antonio, US, and maintains a diverse business portfolio spanning automotive, infrastructure, and industrial sectors worldwide.
Toyota Tsusho has a limited FDA 510(k) regulatory history. The company received 1 FDA 510(k) clearance from 1 total submission, both in 2014. The cleared device falls within the Radiology category. This represents a historical regulatory record; the company has not pursued additional FDA 510(k) submissions in over a decade.
The company's FDA-cleared device was the UNEXEF-38G Ultrasound System, a Radiology device. Toyota Tsusho's involvement in medical device regulation reflects its broader diversification beyond automotive into healthcare and industrial technology sectors.
For detailed information on device names, product codes, and clearance dates, review the complete FDA 510(k) submission record.
FDA 510(k) Regulatory Record - Toyota Tsusho Corporation
1 devices