Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8020300

FEI Number

1000657351

Entity Name

Church & Dwight Canada Corp.

City/State/Country

MONTREAL, QUEBEC, CA

Establishment Address

5485 RUE FERRIER, MONTREAL, QUEBEC --, CA

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

CHURCH & DWIGHT CO., INC. (Owner Number: 2210299)

Owner / Operator Contact Address

500 Charles Ewing Blvd., --, Ewing Township, NJ 08628, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Replens Applicator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUC	Lubricant, Personal	Obstetrics/Gynecology	Class 2	884.5300	2014-10-09

Official Correspondent

No official correspondent registered.

US Agent Details

Lori Barr Business: Church & Dwight Co., Inc. Email: regulatory.na@churchdwight.com Phone: (609) 5033021

Related Public Records

Same Entity

CHURCH & DWIGHT CO., INC.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1122329	Church & Dwight Manufacturing Co., Inc.	South Chesterfield, VA, US
2280705	CHURCH & DWIGHT CO., INC.	PRINCETON, NJ, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K050212	Qualis, Inc.	PERSONAL WARMING JELLY	2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8020300. Last updated year: 2026. Please use registration number 8020300 when referencing this establishment in official correspondence.