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Shanghai Apolo Medical Technology Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
2
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K251031Fiber Laser Treatment Systems (HS-232,HS-233)July 2, 2025
K232409Electromagnetic Stimulation SystemsApril 10, 2024
K221770Fiber Laser Treatment SystemOctober 13, 2022
K203395Platform treatment systemJanuary 28, 2022
K201731Diode Laser Body Sculpture SystemSeptember 10, 2020
K201109CO2 Laser Therapy SystemJuly 15, 2020
K200116PicoSecond Nd: YAG Laser SystemMay 28, 2020
K200746IPL Treatment SystemsMay 15, 2020
K200118Diode Laser Therapy DeviceApril 17, 2020
K191349980nm Diode Laser Therapy DeviceAugust 16, 2019
K190938Phototherapy SystemJune 26, 2019
K190936Q-Switched Nd: YAG Laser SystemJune 17, 2019