Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015908492

FEI Number

3015908492

Entity Name

VETIRUS, LLC

City/State/Country

Naples, FL, US

Establishment Address

4280 Tamiami Trl E Ste 302b, Naples, FL 34112, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Vetirus LLC (Owner Number: 10093921)

Owner / Operator Contact Address

4280 Tamiami Trail E, suite 302 B, Naples, FL 34112, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Blood Collection Kit PLATELET RICH PLASMA SEPARATION KIT Platelet Rich plasma separation kit tube collection capillary blood

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GIO	Tube, Collection, Capillary Blood	Hematology	Class 1	864.6150	2025-08-06

Official Correspondent

Daniela Simic

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vetirus 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 3015908492. Last updated year: 2026. Please use registration number 3015908492 when referencing this establishment in official correspondence.