Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2121746

FEI Number

2121746

Entity Name

Northern Labs Inc

City/State/Country

Manitowoc, WI, US

Establishment Address

5800 West Dr, Manitowoc, WI 54221, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Northern Labs Inc (Owner Number: 10042766)

Owner / Operator Contact Address

5800 West Drive, Manitowoc, WI 54221, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Signet Virex Alpha Gojo ( OTC) Diversity Oxivir Purell ( OTC)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2012-12-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Northern Labs 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 2121746. Last updated year: 2026. Please use registration number 2121746 when referencing this establishment in official correspondence.