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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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