Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022392708

FEI Number

3022392708

Entity Name

INFINITY NEURO, LLC

City/State/Country

Lake Forest, CA, US

Establishment Address

105 North Pointe Drive, Suite A, Lake Forest, CA 92630, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

Infinity Neuro, LLC (Owner Number: 10091089)

Owner / Operator Contact Address

105 North Pointe Drive, Suite A, Lake Forest, CA 92630, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NRY	Catheter, Thrombus Retriever	Cardiovascular	Class 2	870.1250	2024-06-27

Official Correspondent

Ryan Breckenridge

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Infinity Neuro, LLC

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K033736	Concentric Medical, Inc.	MERCI RETRIEVER, MODELS 90065, 90066	2004-08-11

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3008853977	Stryker Neurovascular	Fremont, CA, US
3015615738	Penumbra Inc.	Salt Lake City, UT, US
3016591327	Penumbra Inc.	Roseville, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022392708. Last updated year: 2026. Please use registration number 3022392708 when referencing this establishment in official correspondence.