Seers Technology Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seers Technology Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Seers Technology Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Latest FDA clearance: Jun 2026. Active since 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Seers Technology Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seers Technology Co., Ltd.
2 devices