FDA 510(k) Applications Submitted by Smedtrum Medical Technology Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K230580 03/02/2023 Diode Laser System Smedtrum Medical Technology Co., Ltd.
K231394 05/15/2023 Intense Pulsed Light System Smedtrum Medical Technology Co., Ltd.
K221597 06/02/2022 CO2 Laser System Smedtrum Medical Technology Co., Ltd.


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