WISCONSIN ALUMINUM FOUNDRY CO., INC.

FDA Device Registration & Listing · MANITOWOC, WI, US · Registration 2126663

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
2126663
FEI Number
2126663
Entity Name
WISCONSIN ALUMINUM FOUNDRY CO., INC.
City/State/Country
MANITOWOC, WI, US
Establishment Address
838 S 16th St, MANITOWOC, WI 54220, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Wisconsin Aluminum Foundry Co., Inc. (Owner Number: 2126663)
Owner / Operator Contact Address
838 S 16th St, Manitowoc, WI 54221, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ALL-AMERICAN STERILIZER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FLE Sterilizer, Steam General Hospital Class 2 880.6880 2007-12-05

Official Correspondent

Andy Massignan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Wisconsin Aluminum Foundry Co., 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
K021223 Sauter AG BELIMED STEAM STERILIZER, MODEL TOP 5000 2002-06-26
K050263 M.O. Com S.R.L. MILLENNIUM SERIES, INCLUDING MILLENNIUM B, B+, B2 AND BU 2006-11-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2126663. Last updated year: 2026. Please use registration number 2126663 when referencing this establishment in official correspondence.
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