BEAUXREGARD INDUSTRIES

FDA Device Registration & Listing · Sarasota, FL, US · Registration 3015859108

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
3015859108
FEI Number
3015859108
Entity Name
BEAUXREGARD INDUSTRIES
City/State/Country
Sarasota, FL, US
Establishment Address
1598 Oak Cr. N., Sarasota, FL 34232, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Beauxregard Industries (Owner Number: 10061309)
Owner / Operator Contact Address
2339 Tulip Street, Sarasota, FL 34239, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ViDava ViDava

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FAQ Bag, Urine Collection, Leg, For External Use, Sterile Gastroenterology, Urology Class 1 876.5250 2020-06-22
NNW Bag, Urine Collection, Leg, For External Use, Non-Sterile Gastroenterology, Urology Class 1 876.5250 2022-10-27
EYJ Holder, Ureteral Catheter Gastroenterology, Urology Class 1 876.5130 2019-10-07

Official Correspondent

Daniel Kinsey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Beauxregard Industries
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 3015859108. Last updated year: 2026. Please use registration number 3015859108 when referencing this establishment in official correspondence.
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