Home / Companies / Smedtrum Medical Technology Co., Ltd.

Smedtrum Medical Technology Co., Ltd.

FDA Regulatory Profile

Smedtrum Medical Technology Co., Ltd. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 17, 2024.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240482Intense Pulsed Light System (ST-690)May 17, 2024
K240118Picosecond Nd:YAG Laser SystemApril 30, 2024
K231394Intense Pulsed Light SystemAugust 9, 2023
K230580Diode Laser SystemMay 26, 2023
K221597CO2 Laser SystemSeptember 15, 2022

FDA data resources