Manufacturer registered with FDA
Fissiontech LLC
New York, NY, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 3 510(k) clearances as applicant.
- Device types listed
- 2
- Brands and models
- 6
- 510(k) clearances
- 32024–2025
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 2007–2026
Devices listed with FDA
What Fissiontech LLC currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Anti-Snoring DeviceLRK · Class 2 | Anti-snoring & jaw-repositioning devices | Maker | Advanced Anti Snoring Device 4 Clear/ Advanced Anti Snoring Device 4 BlueBestSelected Anti Snoring DeviceDifiney Advanced Anti Snoring Device 4Difiney Anti Snoring DeviceEXULTIC Anti Snoring Device | 2024 |
| Jaw Repositioning DeviceLQZ · Class 2 | Anti-snoring & jaw-repositioning devices | Maker | Advanced Anti Snoring Device 4 Clear/ Advanced Anti Snoring Device 4 Blue | 2025 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names Fissiontech LLC as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 29 Oct 2025 | K253355 | Difiney Advanced Anti Snoring Device 4.0 | LRK Anti-Snoring Device |
| 8 May 2025 | K250482 | Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue | LRK Anti-Snoring Device |
| 18 Apr 2024 | K233850 | Difiney Anti Snoring Device | LRK Anti-Snoring Device |
Some of these clearances are listed with FDA today by another company: Digital Dental Depot (1), Digital Dental Depot Limited (1).
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| FISSIONTECH LLCFDA reg. 3031978086 | New York, NY, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10091230). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.