SETAGAYA SEIKI Co., Ltd. is one of 136 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
SETAGAYA SEIKI Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DIAMED Handpiece
1
Total
1
Cleared
0
Denied
SETAGAYA SEIKI Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yonezawa-City, JP.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by SETAGAYA SEIKI Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ken Block Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - SETAGAYA SEIKI Co., Ltd.
1 devices