MASDEL INC.

FDA Device Registration & Listing · Anjou Quebec, CA · Registration 3009394814

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
3009394814
FEI Number
3009394814
Entity Name
MASDEL INC.
City/State/Country
Anjou Quebec, CA
Establishment Address
9081 Rue du Parcours, Anjou Quebec H1J2Y1, CA
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Masdel Inc. (Owner Number: 10087855)
Owner / Operator Contact Address
9081 Rue du Parcours, Anjou, CA-QC H1J2Y1, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Supporo Magic Bag

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) General Hospital Class 2 880.5780 2023-04-20
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2023-04-20

Official Correspondent

No official correspondent registered.

US Agent Details

Victoria Pankovich Business: EAS Consulting Group, LLC Email: usagent@easconsultinggroup.com Phone: (571) 4475500

Related Public Records

Same Entity

Masdel 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 3009394814. Last updated year: 2026. Please use registration number 3009394814 when referencing this establishment in official correspondence.
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