Fissiontech, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fissiontech, LLC - FDA 510(k) Cleared Devices
Recent clearances: Difiney Advanced Anti Snoring Device 4.0, Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue, Difiney Anti Snoring Device
3
Total
3
Cleared
0
Denied
Fissiontech, LLC has 3 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Oct 2025. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Fissiontech, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Spica Management Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Fissiontech, LLC
3 devices