Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008191251

FEI Number

3008191251

Entity Name

GENOUROB

City/State/Country

LAVAL Mayenne, FR

Establishment Address

Batiment 60, rue Henri Geret, LAVAL Mayenne 53000, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GENOUROB (Owner Number: 10031129)

Owner / Operator Contact Address

Batiment 60, rue Henri Geret, LAVAL, FR-53 53000, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ROTAB GNRB Dyneelax

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2009-12-23

Official Correspondent

Stephane Nouveau

US Agent Details

Mindy McCann Business: Qserve Group US Inc. Email: usagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

GENOUROB

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 3008191251. Last updated year: 2026. Please use registration number 3008191251 when referencing this establishment in official correspondence.