DASISIMULATIONS, LLC

FDA Device Registration & Listing · Dublin, OH, US · Registration 3030707552

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
3030707552
FEI Number
3030707552
Entity Name
DASISIMULATIONS, LLC
City/State/Country
Dublin, OH, US
Establishment Address
6500 Emerald Pkwy, Suite 200, Dublin, OH 43016, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Dasisimulations, LLC (Owner Number: 10090418)
Owner / Operator Contact Address
6500 Emerald Pkwy, Suite 200, Dublin, OH 43016, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K223809
PMA Number
N/A

All Registered Proprietary Names

PrecisionTAVI

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QQI Interventional Cardiovascular Implant Simulation Software Device Cardiovascular Class 2 870.1405 2024-03-26

Official Correspondent

Manali Shah

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dasisimulations, LLC
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030707552. Last updated year: 2026. Please use registration number 3030707552 when referencing this establishment in official correspondence.
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