Fissiontech LLC
Country not established FDA establishment FEI 3031978086
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- 510(k) 510(k)
Difiney Advanced Anti Snoring Device 4.0 Ref K253355
510(k) 510(k)Difiney Anti Snoring Device Ref K233850
510(k) 510(k)
Company details
- FDA FEI number
- 3031978086
- Address
- 1 Liberty Plz Fl 3, New York, NY, 10006
Frequently asked questions
How many devices does FISSIONTECH LLC have in the registry?
The registry currently lists 3 devices for FISSIONTECH LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list FISSIONTECH LLC's devices?
Among its 3 most recently registered devices, FISSIONTECH LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do FISSIONTECH LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for FISSIONTECH LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from FISSIONTECH LLC in the registry?
The most recently registered devices listed for FISSIONTECH LLC include Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue, Difiney Advanced Anti Snoring Device 4.0 and Difiney Anti Snoring Device.