Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008011247

FEI Number

3008011247

Entity Name

Endologix LLC

City/State/Country

Santa Rosa, CA, US

Establishment Address

3910 Brickway Blvd, Santa Rosa, CA 95403, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Endologix LLC (Owner Number: 9034802)

Owner / Operator Contact Address

3910 Brickway Blvd, Santa Rosa, CA 95403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P220021

All Registered Proprietary Names

Detour System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QWM	Stent Graft, Bypass, Superficial Femoral Artery	Unknown	Class 3	N/A	2023-06-23

Official Correspondent

Kathryn Simpson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Endologix LLC

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3015365904	Endologix LLC	Milpitas, CA, US
3011063223	Endologix LLC	Irvine, CA, US

Similar Registrations

Registration Number	Establishment Name	Location
3015365904	Endologix LLC	Milpitas, CA, US
2030624	Isomedix Operations, Inc.	Temecula, CA, US
3031365458	WOMED SAS	Montpellier Herault, FR
3009999323	STORE-ALL LOGISTICS LTD	Slieverue Kilkenny, IE
3008478369	FERROSAN MEDICAL DEVICES A/S	Soeborg Hovedstaden, DK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008011247. Last updated year: 2026. Please use registration number 3008011247 when referencing this establishment in official correspondence.