Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2133936

FEI Number

3000718675

Entity Name

UROLOGIX, LLC

City/State/Country

Plymouth, MN, US

Establishment Address

13355 10th Ave N., Suite 110, Plymouth, MN 55441, US

Establishment Type(s)

Remanufacture Medical Device,Manufacture Medical Device

Owner / Operator

Urologix LLC (Owner Number: 10051240)

Owner / Operator Contact Address

13355 10th Ave N., Suite 110, Plymouth, MN 55441, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P970008

All Registered Proprietary Names

Coolwave Targis

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	2019-02-04

Official Correspondent

Mark Swanson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Urologix LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3009969279	Medifocus Inc	Columbia, MD, US
3007029079	AMPHENOL ALDEN PRODUCTS COMPANY	Hermosillo Sonora, MX
1721686	Sterigenics U.S., LLC	Santa Teresa, NM, US
3010806653	MediConcepts Technology (Shenzhen) Company Limited	Shenzhen Guangdong, CN
1721676	Sterigenics U.S., LLC	Salt Lake City, UT, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2133936. Last updated year: 2026. Please use registration number 2133936 when referencing this establishment in official correspondence.