PREVENT PLUS, LLC.

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3012669304

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012669304
FEI Number
3012669304
Entity Name
PREVENT PLUS, LLC.
City/State/Country
Saint Louis, MO, US
Establishment Address
4220 Duncan Ave, Suite 201, Saint Louis, MO 63110, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Prevent-Plus, LLC (Owner Number: 10052036)
Owner / Operator Contact Address
4220 Duncan Ave Suite 201, Saint Louis, MO 63110, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K032948
PMA Number
N/A

All Registered Proprietary Names

Preventogen

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMF Bandage, Liquid General Hospital Class 1 880.5090 2016-06-03

Official Correspondent

Brad Chartrand

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Prevent-Plus, LLC
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 3012669304. Last updated year: 2026. Please use registration number 3012669304 when referencing this establishment in official correspondence.
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