Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004956832

FEI Number

3004956832

Entity Name

I-MED PHARMA INC.

City/State/Country

St Laurent Quebec, CA

Establishment Address

7190 Fredrick Banting Rd., St Laurent Quebec H4S 2A1, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

I-MED Pharma Inc. (Owner Number: 10072828)

Owner / Operator Contact Address

7190 Frederick Banting Rd., Saint-Laurent, CA-QC H4S 2A1, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

I-RELIEF

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2020-06-10

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

I-MED Pharma 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 3004956832. Last updated year: 2026. Please use registration number 3004956832 when referencing this establishment in official correspondence.