VITAL GUARD PHARMA

FDA Device Registration & Listing · Butler, WI, US · Registration 3040999009

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
3040999009
FEI Number
3040999009
Entity Name
VITAL GUARD PHARMA
City/State/Country
Butler, WI, US
Establishment Address
4554 N 126th St, Butler, WI 53007, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
VITAL GUARD PHARMA (Owner Number: 10093628)
Owner / Operator Contact Address
4554 n 126th street Butler, Butler, WI 53007, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dario - 100 Count Relion Prime/Premier 50ct PRECISION XTRA KETONE STRIPS- 10CT AccuChek Guide 25ct or NFR (yellow stripe)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OCR Lung Sound Monitor Cardiovascular Class 2 870.1875 2026-03-28

Official Correspondent

Austin Hamill

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VITAL GUARD PHARMA
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 3040999009. Last updated year: 2026. Please use registration number 3040999009 when referencing this establishment in official correspondence.
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