AVENTUSOFT

FDA Device Registration & Listing · Boca Raton, FL, US · Registration 3029300449

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
3029300449
FEI Number
3029300449
Entity Name
AVENTUSOFT
City/State/Country
Boca Raton, FL, US
Establishment Address
3651 FAU Blvd, Suite 300, Boca Raton, FL 33431, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Aventusoft, LLC (Owner Number: 10088690)
Owner / Operator Contact Address
3651 FAU Blvd, Suite 300, Boca Raton, FL 33431, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HEMOTAG CLINICAL DASHBOARD HEMOTAG MOBILE APP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUG Medical Device Data System General Hospital Class 1 880.6310 2023-10-11

Official Correspondent

Gary Becker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aventusoft, 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 3029300449. Last updated year: 2026. Please use registration number 3029300449 when referencing this establishment in official correspondence.
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