Senbitec Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Senbitec Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: HESTIA (L200-A)
1
Total
1
Cleared
0
Denied
Senbitec Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Anyang-Si, KR.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Senbitec Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtech Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Senbitec Co., Ltd.
1 devices