ClearanceBrief
Company ยท TW

Smedtrum Medical Technology Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2024. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEXPowered Laser Surgical Instrument3
ONFPowered Light Based Non-Laser Surgical Instrument With Thermal Effect2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 17, 2024K240482Intense Pulsed Light System (ST-690)
Smedtrum Medical Technology Co., Ltd., TW
ONF
Apr 30, 2024K240118Picosecond Nd:YAG Laser System
Smedtrum Medical Technology Co., Ltd., TW
GEX
Aug 9, 2023K231394Intense Pulsed Light System
Smedtrum Medical Technology Co., Ltd., TW
ONF
May 26, 2023K230580Diode Laser System
Smedtrum Medical Technology Co., Ltd., TW
GEX
Sep 15, 2022K221597CO2 Laser System
Smedtrum Medical Technology Co., Ltd., TW
GEX

Latest recalls

DateFirm and productCodeLinked 510(k)
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