Sangi Co, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sangi Co, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sangi Co, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
2 devices