WEIMAN PRODUCTS, LLC

FDA Device Registration & Listing · GURNEE, IL, US · Registration 1450386

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
1450386
FEI Number
1416404
Entity Name
WEIMAN PRODUCTS, LLC
City/State/Country
GURNEE, IL, US
Establishment Address
755 Tri State Pkwy, GURNEE, IL 60031, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
WEIMAN PRODUCTS, LLC (Owner Number: 9914067)
Owner / Operator Contact Address
755 TRI STATE PARKWAY, --, Gurnee, IL 60031, US
Initial Importer Flag
N
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
MED Sterilant, Medical Devices General Hospital Class 2 880.6885 2011-07-22
JOJ Indicator, Physical/Chemical Sterilization Process General Hospital Class 2 880.2800 2019-08-29
JCB Detergent Pathology Class 1 864.4010 2025-04-23
KOX Solvent, Adhesive Tape General, Plastic Surgery Class 1 878.4730 1992-06-15
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2008-03-06

Official Correspondent

Charles Reedy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WEIMAN PRODUCTS, 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
K033381 Discus Dental, Inc. DISCHEM CHEMICAL PROPORTIONING & DISPENSING SYSTEM FOR USE WITH CETYLCIDE-G CONCENTRATE AND DILUENT, AQUARIUS MODEL 2004-01-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2007 N/A 2
3M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S and STERRAD 50 Sterilization Systems. Indicator for hydrogen peroxide sterilant.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1450386. Last updated year: 2026. Please use registration number 1450386 when referencing this establishment in official correspondence.
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