Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016566173

FEI Number

3016566173

Entity Name

KINVENT BIOMECANIQUE

City/State/Country

Montepellier Herault, FR

Establishment Address

6 Rue de Pommessargues, Montepellier Herault 34000, FR

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device,Repack or Relabel Medical Device

Owner / Operator

Kinvent Biomecanique SAS (Owner Number: 10062556)

Owner / Operator Contact Address

6 Rue de Pommessargues, Montepellier, FR-34 34000, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

K-LAB K-INVENT K-Invent K-Delta K-FORCE K-Force KINVENT KFORCE K-Push K-Pull K-Bubble K-Deltas XL K-Grip K-Move K-Deltas K-Force Plates K Myo Accessories K Myo x1000 patches pack K-myo x1000 patches pack K-LAB KINVENT K-Force K-INVENT K-Delta K-FORCE KFORCE K-Invent K-Push K-Pull K-Force Plates K-Bubble K-Grip K-Deltas K-Move K-Deltas XL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HRW	Dynamometer, Nonpowered	Orthopedic	Class 1	888.1250	2020-02-13
DRX	Electrode, Electrocardiograph	Cardiovascular	Class 2	870.2360	2024-05-16
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2020-02-13

Official Correspondent

Emmanouil Athanasopoulos

US Agent Details

Mohsen Aminipour Business: FDA Listing Inc. Email: info@fdalisting.com Phone: (646) 5124798

Related Public Records

Same Entity

Kinvent Biomecanique SAS

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
K934333	3M Medical Products Group	3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE	1994-07-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016566173. Last updated year: 2026. Please use registration number 3016566173 when referencing this establishment in official correspondence.