Sangi Co, Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Sangi Co, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste), Apapro Desensitizer
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.
FDA 510(k) Regulatory Record - Sangi Co, Ltd.
2 devices