Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010457124

FEI Number

3010457124

Entity Name

KNIX WEAR, INC.

City/State/Country

Toronto Ontario, CA

Establishment Address

179 John St, #600, Toronto Ontario M5T 1X4, CA

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Knix Wear, Inc. (Owner Number: 10082493)

Owner / Operator Contact Address

179 John St, # 600, Toronto, CA-ON M5T 1X4, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Knix Knix

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	2021-08-04
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2021-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

Drashti Desai Email: Regulatory@knix.com Phone: (704) 7311115

Related Public Records

Same Entity

Knix Wear, Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010457124. Last updated year: 2026. Please use registration number 3010457124 when referencing this establishment in official correspondence.