THE HARLOFF COMPANY, INC.

FDA Device Registration & Listing · Colorado Springs, CO, US · Registration 3001109397

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3001109397
FEI Number
3001109397
Entity Name
THE HARLOFF COMPANY, INC.
City/State/Country
Colorado Springs, CO, US
Establishment Address
650 Ford Street, Colorado Springs, CO 80915, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
The Harloff Company, Inc. (Owner Number: 10032938)
Owner / Operator Contact Address
650 Ford Street, Colorado Springs, CO 80915, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

M-Series A-Series A-Series M-Series

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZN Cart, Emergency, Cardiopulmonary (Excluding Equipment) Anesthesiology Class 1 868.6175 2010-10-11
BRY Cabinet, Table And Tray, Anesthesia Anesthesiology Class 1 868.6100 2025-02-04

Official Correspondent

Kelly Robinson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Harloff Company, 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 3001109397. Last updated year: 2026. Please use registration number 3001109397 when referencing this establishment in official correspondence.
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