FISSIONTECH LLC

FDA Device Registration & Listing · New York, NY, US · Registration 3031978086

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3031978086
FEI Number
3031978086
Entity Name
FISSIONTECH LLC
City/State/Country
New York, NY, US
Establishment Address
1 Liberty Plz Fl 3, New York, NY 10006, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Fissiontech LLC (Owner Number: 10091230)
Owner / Operator Contact Address
1 Liberty Plz FL 3, New York, NY 10006, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250482
PMA Number
N/A

All Registered Proprietary Names

Difiney Advanced Anti Snoring Device 4 Advanced Anti Snoring Device 4 Clear/ Advanced Anti Snoring Device 4 Blue

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRK Device, Anti-Snoring Dental Class 2 872.5570 2026-02-13
LRK Device, Anti-Snoring Dental Class 2 872.5570 2025-06-19
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2025-06-19

Official Correspondent

Mike Lee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fissiontech LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031978086. Last updated year: 2026. Please use registration number 3031978086 when referencing this establishment in official correspondence.
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