Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030926983

FEI Number

3030926983

Entity Name

TOEFX INC.

City/State/Country

Hamilton Ontario, CA

Establishment Address

1280 Main Street West, Building #039, Suite B129, Hamilton Ontario L8S 4M3, CA

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

ToeFx Inc. (Owner Number: 10090589)

Owner / Operator Contact Address

1280 Main Street West, Building #039, Suite B129, Hamilton, CA-ON L8S 4M3, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TFX-LT2000 Therapy Light FungalBlue

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PDZ	Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis	General, Plastic Surgery	Class 2	878.4810	2024-04-16
FZZ	Marker, Skin	General, Plastic Surgery	Class 1	878.4660	2025-12-01

Official Correspondent

No official correspondent registered.

US Agent Details

Roshana Ahmed Business: QUARAS, LLC Email: rahmed@quarasconsulting.com Phone: (657) 2487361

Related Public Records

Same Entity

ToeFx Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030926983. Last updated year: 2026. Please use registration number 3030926983 when referencing this establishment in official correspondence.