Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023356343

FEI Number

3023356343

Entity Name

DORIGO SYSTEMS LTD.

City/State/Country

Burnaby British Columbia, CA

Establishment Address

5085 North Fraser Way, Dorigo Systems, Burnaby British Columbia V5J0J2, CA

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Dorigo Systems Ltd. (Owner Number: 10095023)

Owner / Operator Contact Address

5085 North Fraser Way, Dorigo Systems, Burnaby, CA-BC V5J0J2, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Myolift MD Myolift 600+ Myolift Mini UltraBeauty Myolift Myolift TW Myolift 600 Myolift Ultra

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NFO	Stimulator, Transcutaneous Electrical, Aesthetic Purposes	Neurology	Class 2	882.5890	2026-01-21

Official Correspondent

Mark Pillon

US Agent Details

Taylor Wagemans Business: HCW Sales LLC Email: taylor@hcwassoc.com Phone: (253) 9735019

Related Public Records

Same Entity

Dorigo Systems Ltd.

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 3023356343. Last updated year: 2026. Please use registration number 3023356343 when referencing this establishment in official correspondence.