SIM&CURE

FDA Device Registration & Listing · Montpellier Herault, FR · Registration 3015978024

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
3015978024
FEI Number
3015978024
Entity Name
SIM&CURE
City/State/Country
Montpellier Herault, FR
Establishment Address
95 rue Pierre Flourens, Batiment H, Montpellier Herault 34090, FR
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
SIM&CURE (Owner Number: 10061464)
Owner / Operator Contact Address
95 rue Pierre Flourens, Batiment H, Montpellier, FR-34 34090, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Sim&Size Sim&Size Sim&Size SIM&SIZE SIM&SIZE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PZO Software For Visualization Of Vascular Anatomy And Intravascular Devices Radiology Class 2 892.2050 2025-01-28
PZO Software For Visualization Of Vascular Anatomy And Intravascular Devices Radiology Class 2 892.2050 2019-10-21
PZO Software For Visualization Of Vascular Anatomy And Intravascular Devices Radiology Class 2 892.2050 2023-03-13
PZO Software For Visualization Of Vascular Anatomy And Intravascular Devices Radiology Class 2 892.2050 2021-05-26
PZO Software For Visualization Of Vascular Anatomy And Intravascular Devices Radiology Class 2 892.2050 2022-05-16

Official Correspondent

Mathieu SANCHEZ

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

SIM&CURE
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K250160 Mentice Spain S.L. ANKYRAS 2025-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015978024. Last updated year: 2026. Please use registration number 3015978024 when referencing this establishment in official correspondence.
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