Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012696653

FEI Number

3012696653

Entity Name

VENTUREMED GROUP, Inc

City/State/Country

Plymouth, MN, US

Establishment Address

2800 Campus Dr., Suite 50, Plymouth, MN 55441, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

VentureMed Group, Inc. (Owner Number: 10052004)

Owner / Operator Contact Address

2800 Campus Drive, Suite 50, Plymouth, MN 55441, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K202187

PMA Number

N/A

All Registered Proprietary Names

FLEX Vessel Prep System FLEX Vessel Prep System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PNO	Catheter, Percutaneous, Cutting/Scoring	Cardiovascular	Class 2	870.1250	2016-05-31
PNO	Catheter, Percutaneous, Cutting/Scoring	Cardiovascular	Class 2	870.1250	2025-12-05

Official Correspondent

Jill Schweiger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VentureMed Group, 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 3012696653. Last updated year: 2026. Please use registration number 3012696653 when referencing this establishment in official correspondence.