Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015099059

FEI Number

3015099059

Entity Name

DERMADRY LABORATORIES INC.

City/State/Country

Montreal Quebec, CA

Establishment Address

5824, Rue D'Iberville, Montreal Quebec H2G2B9, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Dermadry Laboratories Inc. (Owner Number: 10062723)

Owner / Operator Contact Address

5824, Rue D'Iberville, Montreal, CA-QC H2G2B9, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K192749

PMA Number

N/A

All Registered Proprietary Names

Dermadry - Underarms Dermadry - Total Dermadry - Hands and Feet

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EGJ	Device, Iontophoresis, Other Uses	Physical Medicine	Class 2	890.5525	2020-03-04

Official Correspondent

Mohamed Amine Daoud

US Agent Details

Marilyne Joly Business: LOK USA, Inc. Email: regulatory@lok-northamerica.com Phone: (412) 2851076

Related Public Records

Same Entity

Dermadry Laboratories Inc.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K842483	Santa Barbara Medco, Inc.	SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC	1984-08-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015099059. Last updated year: 2026. Please use registration number 3015099059 when referencing this establishment in official correspondence.