FDA 510(k) Applications Submitted by Lotuxs Medtech (Suzhou) Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K211402 05/06/2021 Powersculp laser lipolysis system Lotuxs Medtech (Suzhou) Co., Ltd.
K222862 09/22/2022 SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC Lotuxs Medtech (Suzhou) Co., Ltd.


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