WEB-TEX, INC.

FDA Device Registration & Listing · MONTREAL, Quebec, CA · Registration 8043782

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
8043782
FEI Number
3001585912
Entity Name
WEB-TEX, INC.
City/State/Country
MONTREAL, Quebec, CA
Establishment Address
9400 Saint Laurent, Suite 300, MONTREAL, Quebec H2N IP3, CA
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
WEB-TEX, INC. (Owner Number: 9003778)
Owner / Operator Contact Address
9400 Saint Laurent, Suite 300, Montreal, CA-QC H2N IP3, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Adhesive Tape and Bandage Reusable Hot and Cold Pack WEB-TEX TUBULAR COTTON STOCKINETTE Gauze Support Absorbent cotton roll Support

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2003-04-07
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2007-08-22
FQL Stocking, Medical Support (For General Medical Purposes) General Hospital Class 1 880.5780 1998-04-28
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2012-05-02
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2017-05-02
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2014-03-21
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2017-05-02

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

WEB-TEX, 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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043782. Last updated year: 2026. Please use registration number 8043782 when referencing this establishment in official correspondence.
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