DESKi SAS

FDA Device Registration & Listing · Bordeaux Nouvelle-Aquitaine, FR · Registration 3040362673

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
3040362673
FEI Number
3040362673
Entity Name
DESKi SAS
City/State/Country
Bordeaux Nouvelle-Aquitaine, FR
Establishment Address
2 Place de la Bourse, Bordeaux Nouvelle-Aquitaine 33000, FR
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
DESKi (Owner Number: 10093963)
Owner / Operator Contact Address
2 Place de la Bource, Bordeaux, FR-NAQ 33000, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

HeartFocus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QJU Image Acquisition And/Or Optimization Guided By Artificial Intelligence Radiology Class 2 892.2100 2026-06-17

Official Correspondent

No official correspondent registered.

US Agent Details

Kelly Porfirio Email: kelly.porfirio@deski.ai Phone: (516) 2998071

Related Public Records

Same Entity

DESKi
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 3040362673. Last updated year: 2026. Please use registration number 3040362673 when referencing this establishment in official correspondence.
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