Medimaps Group SA

FDA Device Registration & Listing · Plan-les-Ouates Geneve, CH · Registration 3010208539

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
3010208539
FEI Number
3010208539
Entity Name
Medimaps Group SA
City/State/Country
Plan-les-Ouates Geneve, CH
Establishment Address
36A Chemin Du Champ des Filles, Plan-les-Ouates Geneve CH-1228, CH
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Medimaps SA (Owner Number: 10042744)
Owner / Operator Contact Address
HiFlow 36A Chemin Du Champ des Filles, Plan-Les-Ouates, CH-GE 1228, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K243218
PMA Number
N/A

All Registered Proprietary Names

TBS iNsight (V4)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGI Densitometer, Bone Radiology Class 2 892.1170 2025-01-28

Official Correspondent

No official correspondent registered.

US Agent Details

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

Related Public Records

Same Entity

Medimaps SA
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
K983273 Medical Systems, Inc. XCT 2000 L PQCT BONE DENSITOMETER 1998-10-29

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010208539. Last updated year: 2026. Please use registration number 3010208539 when referencing this establishment in official correspondence.
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