Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9613808

FEI Number

3003052208

Entity Name

GH GUNTHER HUETTLIN MANUFACTURING, INC.

City/State/Country

BELLEVILLE Ontario, CA

Establishment Address

101 PETRIE PL., BELLEVILLE Ontario K8N 5T3, CA

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

GH GUNTHER HUETTLIN MANUFACTURING, INC. (Owner Number: 9041378)

Owner / Operator Contact Address

101 PETRIE PL., --, BELLEVILLE, ONTARIO, CA-NOTA K8N 5T3, 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
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2000-05-18
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2024-11-04

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

GH GUNTHER HUETTLIN MANUFACTURING, 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
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 9613808. Last updated year: 2026. Please use registration number 9613808 when referencing this establishment in official correspondence.