VENOSCOPE, LLC

FDA Device Registration & Listing · LAFAYETTE, LA, US · Registration 2319429

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
2319429
FEI Number
1000306918
Entity Name
VENOSCOPE, LLC
City/State/Country
LAFAYETTE, LA, US
Establishment Address
1018 HARDING ST STE 104, LAFAYETTE, LA 70503, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
VENOSCOPE, LLC (Owner Number: 9010689)
Owner / Operator Contact Address
1018 HARDING ST., SUITE 104, --, Lafayette, LA 70503, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K941035
PMA Number
N/A

All Registered Proprietary Names

Venoscope VT03

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HJN Transilluminator, Battery-Powered Ophthalmic Class 1 886.1945 2020-03-05

Official Correspondent

FRANK CREAGHAN, JR.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VENOSCOPE, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2319429. Last updated year: 2026. Please use registration number 2319429 when referencing this establishment in official correspondence.
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