# Fissiontech, LLC

- Location (FDA's records): New York, NY
- FDA decisions: 3 (2024–2025): 3 510(k) clearances
- Product codes: LRK (3)
- 510(k) review time since 2016: median 78 days, against 107 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Apnea Sciences Corporation: 1 (https://510kreport.com/company/apnea-sciences)

## Firms that cite its devices most
- Endeavor Commerce, LLC: 1 (https://510kreport.com/company/endeavor-commerce)

## Its most-cited devices
- K233850: Difiney Anti Snoring Device (2024), cited by 2
- K250482: Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue (2025), cited by 1

## Recent decisions
- K253355: Difiney Advanced Anti Snoring Device 4.0 (Oct 29, 2025)
- K250482: Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue (May 8, 2025)
- K233850: Difiney Anti Snoring Device (Apr 18, 2024)

Source page: https://510kreport.com/company/fissiontech