Seers Technology Co., Ltd. is one of 13048 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
Recent clearances: mobiCARE Cardiac Monitoring System (mobiCARE-MC200M, mobiCARE-MC200ML, mobiCARE-MC200M7, mobiCARE-MC200ML7), HX-461
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.
510(k) submissions have been managed by Cardiovascular Biometrics Sourcing, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Seers Technology Co., Ltd.
2 devices