Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1954553

FEI Number

3003273873

Entity Name

I.V. HOUSE

City/State/Country

Saint Louis, MO, US

Establishment Address

2072 Concourse Dr, Saint Louis, MO 63146, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

I.V. HOUSE, INC. (Owner Number: 9044986)

Owner / Operator Contact Address

2072 Concourse Dr, --, Saint Louis, MO 63146, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

I.V. HOUSE ULTRADRESSING I.V. HOUSE ULTRADOME I.V. HOUSE INTRAVEN

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2001-03-07

Official Correspondent

Peter Vallino

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

I.V. HOUSE, 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 1954553. Last updated year: 2026. Please use registration number 1954553 when referencing this establishment in official correspondence.