GladRags

FDA Device Registration & Listing · PORTLAND, OR, US · Registration 3032370

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3032370
FEI Number
3001741512
Entity Name
GladRags
City/State/Country
PORTLAND, OR, US
Establishment Address
2345 N Ross Ave, PORTLAND, OR 97227, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GR Biz LLC (Owner Number: 9032881)
Owner / Operator Contact Address
2345 N Ross Ave, Portland, OR 97227, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GladRags GladRags

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUQ Pad, Menstrual, Reusable Obstetrics/Gynecology Class 1 884.5435 2025-07-22
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 1998-02-04

Official Correspondent

Sara Tunstall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GR Biz LLC
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 3032370. Last updated year: 2026. Please use registration number 3032370 when referencing this establishment in official correspondence.
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