Vaporox Headquarters

FDA Device Registration & Listing · Lone Tree, CO, US · Registration 3015423531

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
3015423531
FEI Number
3015423531
Entity Name
Vaporox Headquarters
City/State/Country
Lone Tree, CO, US
Establishment Address
8375 S. Willow Street, Ste. 500, Lone Tree, CO 80124, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Vaporox Inc. (Owner Number: 10059868)
Owner / Operator Contact Address
8375 Willow Street, Ste. 500, Lone Tree, CO 80124, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

VHT-200

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPJ Chamber, Oxygen, Topical, Extremity General, Plastic Surgery Class 2 878.5650 2025-06-04

Official Correspondent

Alan Sage

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vaporox 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 3015423531. Last updated year: 2026. Please use registration number 3015423531 when referencing this establishment in official correspondence.
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