Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2183494

FEI Number

2183494

Entity Name

BEFOUR, INC.

City/State/Country

SAUKVILLE, WI, US

Establishment Address

102 PROGRESS DR., SAUKVILLE, WI 53080, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BEFOUR, INC. (Owner Number: 2183494)

Owner / Operator Contact Address

102 PROGRESS DR., --, Saukville, WI 53080, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Befour MX115,170,305,350

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRW	Scale, Patient	General Hospital	Class 1	880.2720	1992-07-10

Official Correspondent

GARY BUTTERS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BEFOUR, 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 2183494. Last updated year: 2026. Please use registration number 2183494 when referencing this establishment in official correspondence.