Medical Device Manufacturer · JP , Himeji, Hyogo

Takiron Co., Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2007

Total

Cleared

Denied

Takiron Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Himeji, Hyogo, JP.

Historical record: 6 cleared submissions from 2007 to 2008. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Takiron Co., Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Takiron Co., Ltd.

6 devices

1-6 of 6