DESSINTEY

FDA Device Registration & Listing · SAINT JEAN BONNEFONDS Loire, FR · Registration 3020897597

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
3020897597
FEI Number
3020897597
Entity Name
DESSINTEY
City/State/Country
SAINT JEAN BONNEFONDS Loire, FR
Establishment Address
Parc Technologique METROTECH, Batiment 6, SAINT JEAN BONNEFONDS Loire 42650, FR
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
DESSINTEY (Owner Number: 10083127)
Owner / Operator Contact Address
Parc Technologique METROTECH, Batiment 6, SAINT JEAN BONNEFONDS, FR-42 42650, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

IVS3 IVS4

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKC Interactive Rehabilitation Exercise Device, Prescription Use Physical Medicine Class 2 890.5360 2021-11-08

Official Correspondent

JEROME MARNAS

US Agent Details

Robert Packard Business: Medical Device Academy Incorporated Email: rob@fdaestar.com Phone: (802) 2581881

Related Public Records

Same Entity

DESSINTEY
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 3020897597. Last updated year: 2026. Please use registration number 3020897597 when referencing this establishment in official correspondence.
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