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Fissiontech, LLC

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K253355Difiney Advanced Anti Snoring Device 4.0October 29, 2025
K250482Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 BlueMay 8, 2025
K233850Difiney Anti Snoring DeviceApril 18, 2024