Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002900281

FEI Number

3002900281

Entity Name

LUNDELL MANUFACTURING CORP.

City/State/Country

Minneapolis, MN, US

Establishment Address

2700 Ranchview Ln N, Minneapolis, MN 55447, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Lundell Manufacturing Corp. (Owner Number: 10051706)

Owner / Operator Contact Address

2700 Ranchview Lane, Minneapolis, MN 55447, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBL	Absorbent, Carbon-Dioxide	Anesthesiology	Class 1	868.5300	2016-04-22

Official Correspondent

Mark Streiff

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lundell Manufacturing Corp.

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 3002900281. Last updated year: 2026. Please use registration number 3002900281 when referencing this establishment in official correspondence.