Shenzhen Future Electronic Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251662Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression ThNovember 13, 2025
K221092Transcutaneous Electrical Nerve Stimulator Model: ST-304September 13, 2022
K213745Air Compression Therapy Device, model: ST-502March 31, 2022