Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008147479

FEI Number

3008147479

Entity Name

J. BRASCH CO LLC

City/State/Country

Lincoln, NE, US

Establishment Address

1620 North 20th Circle, Lincoln, NE 68503, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

JBrasch Co., LLC (Owner Number: 10030835)

Owner / Operator Contact Address

1620 North 20th Circle, Lincoln, NE 68503, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SURE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMI	Monitor, Bed Patient	General Hospital	Class 1	880.2400	2009-12-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JBrasch Co., LLC

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 3008147479. Last updated year: 2026. Please use registration number 3008147479 when referencing this establishment in official correspondence.