Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9681878

FEI Number

3003341973

Entity Name

FEMPRO Consumer Products ULC

City/State/Country

DRUMMONDVILLE Quebec, CA

Establishment Address

1330 Jean-Berchmans-Michaud, DRUMMONDVILLE Quebec J2C 2Z5, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Fempro Consumer Products ULC (Owner Number: 9027945)

Owner / Operator Contact Address

1330 Jean-Berchmans-Michaud, --, DRUMMONDVILLE, CA-QC J2C 2Z5, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2016-08-25
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2022-07-25
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	1996-09-20

Official Correspondent

No official correspondent registered.

US Agent Details

Linda Honda Email: LHonda@firstquality.com Phone: (570) 3670354

Related Public Records

Same Entity

Fempro Consumer Products ULC

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
K823241	Kimberly-Clark Corp.	NEW FREEDOM THIN UNSCENTED MAXI PADS	1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9681878. Last updated year: 2026. Please use registration number 9681878 when referencing this establishment in official correspondence.