Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3034538367

FEI Number

3034538367

Entity Name

MODULATE TECHNOLOGIES INC

City/State/Country

Montreal Quebec, CA

Establishment Address

800 Rue du Square-Victoria, Suite 433, Montreal Quebec H3C 0B4, CA

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Modulate Technologies Inc (Owner Number: 10091991)

Owner / Operator Contact Address

800 Rue du Square-Victoria, Suite 433, Montreal, CA-QC H3C 0B4, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Modulate Brace Modulate Brace

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IQE	Orthosis, Lumbar	Physical Medicine	Class 1	890.3490	2024-11-22
IPT	Orthosis, Thoracic	Physical Medicine	Class 1	890.3490	2024-11-22

Official Correspondent

Aymeric Guy

US Agent Details

Stephan Toupin Business: Dawa Medical LLC Email: stoupin@dawamedical.com Phone: (305) 5999373

Related Public Records

Same Entity

Modulate Technologies 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 3034538367. Last updated year: 2026. Please use registration number 3034538367 when referencing this establishment in official correspondence.