Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014146191

FEI Number

3014146191

Entity Name

PHRAXIS INC

City/State/Country

Minneapolis, MN, US

Establishment Address

333 Hennepin Ave E, Unit 1903, Minneapolis, MN 55414, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Phraxis Inc (Owner Number: 10093541)

Owner / Operator Contact Address

333 Hennepin Ave E, Unit 1903, Minneapolis, MN 55414, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P240004

All Registered Proprietary Names

EndoForce Connector for Endovascular Venous Anastomosis

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SEQ	Covered Stent Vascular Connector, Hemodialysis Access Circuit	Unknown	Class 3	N/A	2025-05-31

Official Correspondent

John Zentgraf

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Phraxis 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 3014146191. Last updated year: 2026. Please use registration number 3014146191 when referencing this establishment in official correspondence.