AVICENA LLC DBA VENTRIC HEALTH

FDA Device Registration & Listing · Pasadena, CA, US · Registration 3018772859

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
3018772859
FEI Number
3018772859
Entity Name
AVICENA LLC DBA VENTRIC HEALTH
City/State/Country
Pasadena, CA, US
Establishment Address
117 E Colorado Blvd., Suite 510, Pasadena, CA 91105, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Avicena LLC DBA Ventric Health (Owner Number: 10088868)
Owner / Operator Contact Address
117 E Colorado Blvd., Suite 510, Pasadena, CA 91105, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223905
PMA Number
N/A

All Registered Proprietary Names

Vivio System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QUO Adjunctive Heart Failure Status Indicator Cardiovascular Class 2 870.2200 2023-10-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Avicena LLC DBA Ventric Health
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 3018772859. Last updated year: 2026. Please use registration number 3018772859 when referencing this establishment in official correspondence.
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