Lotuxs Medtech (Suzhou) Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Lotuxs Medtech (Suzhou) Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC, Powersculp laser lipolysis system
2
Total
2
Cleared
0
Denied
Lotuxs Medtech (Suzhou) Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Suzhou, CN.
Last cleared in 2023. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lotuxs Medtech (Suzhou) Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lotuxs Medtech (Suzhou) Co., Ltd.
2 devices