Endologix LLC

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3015365904

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
3015365904
FEI Number
3015365904
Entity Name
Endologix LLC
City/State/Country
Milpitas, CA, US
Establishment Address
1971 Milmont Dr, Milpitas, CA 95035, US
Establishment Type(s)
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
N
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
3011063223 Endologix LLC Irvine, CA, US
3008011247 Endologix LLC Santa Rosa, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015365904. Last updated year: 2026. Please use registration number 3015365904 when referencing this establishment in official correspondence.
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