Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2182202

FEI Number

2182202

Entity Name

VOLLRATH COMPANY LLC, THE

City/State/Country

Sheboygan, WI, US

Establishment Address

1236 N 18TH ST, Sheboygan, WI 53081, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

The Vollrath Co., LLC (Owner Number: 2183714)

Owner / Operator Contact Address

502 Hwy. 67, --, Kiel, WI 53042, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Polar Ware

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FNP	Urinal	General Hospital	Class 1	880.6730	2009-06-05
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2015-06-22
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	1992-07-02
FOB	Bedpan	General Hospital	Class 1	880.6730	1992-07-02
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	1992-07-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Vollrath Co., LLC

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
2183714	The Vollrath Company LLC	Kiel, WI, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2182202. Last updated year: 2026. Please use registration number 2182202 when referencing this establishment in official correspondence.