Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007972010

FEI Number

3007972010

Entity Name

CVRX, INC.

City/State/Country

Minneapolis, MN, US

Establishment Address

9201 W Broadway Ave Ste 650, Minneapolis, MN 55445, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CVRx, Inc. (Owner Number: 10034991)

Owner / Operator Contact Address

9201 West Broadway Avenue, Suite 650, Minneapolis, MN 55445, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P180050

All Registered Proprietary Names

Barostim System, Barostim, Barostim NEO2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DSR	Stimulator, Carotid Sinus Nerve	Cardiovascular	Class 3	870.3850	2019-09-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CVRx, Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007972010. Last updated year: 2026. Please use registration number 3007972010 when referencing this establishment in official correspondence.