Medifocus Inc

FDA Device Registration & Listing · Columbia, MD, US · Registration 3009969279

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
3009969279
FEI Number
3009969279
Entity Name
Medifocus Inc
City/State/Country
Columbia, MD, US
Establishment Address
9150 Rumsey Road Suite A4, Columbia, MD 21045, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Medifocus Inc (Owner Number: 10042433)
Owner / Operator Contact Address
9150 Rumsey Road, Suite A4, Columbia, MD 21045, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P030006

All Registered Proprietary Names

Prolieve Thermodilatation System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MEQ System, Hyperthermia, Rf/Microwave (Benign Prostatic Hyperplasia),Thermotherapy Unknown Class 3 N/A 2012-11-27

Official Correspondent

Douglas Liu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Medifocus Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009969279. Last updated year: 2026. Please use registration number 3009969279 when referencing this establishment in official correspondence.
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