Data / Medical devices / United States / Fissiontech LLC
Fissiontech LLC: FDA-registered device maker in New York, NY, United States, 3 510(k) clearances
Fissiontech LLC is registered with the FDA (registration 3031978086) in New York, NY, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 29, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031978086
- Address
- 1 Liberty Plz Fl 3, New York, NY, United States, 10006
- Owner or operator
- Fissiontech LLC (10091230)
- Roles
- Manufacturer
- First device listed
- July 28, 2024
- Registered through
- 2026
- Brand names listed
- Advanced Anti Snoring Device 4 Clear/ Advanced Anti Snoring Device 4 Blue, BestSelected Anti Snoring Device, Difiney Advanced Anti Snoring Device 4, Difiney Anti Snoring Device, EXULTIC Anti Snoring Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Anti-Snoring | LRK | 2 | Manufacturer | accessdata.fda.gov |
| Device, Jaw Repositioning | LQZ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 29, 2025 | K253355 | Difiney Advanced Anti Snoring Device 4.0 | LRK | Substantially Equivalent | Fissiontech, LLC | accessdata.fda.gov |
| May 8, 2025 | K250482 | Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue | LRK | Substantially Equivalent | Fissiontech, LLC | accessdata.fda.gov |
| April 18, 2024 | K233850 | Difiney Anti Snoring Device | LRK | Substantially Equivalent | Fissiontech, LLC | accessdata.fda.gov |
Compare with other makers
Updated October 29, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.