# KINVENT BIOMECANIQUE

FEI: 3016566173
Status: Active
Establishment types: Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Kinvent Biomecanique SAS (#10062556)

Address: 6 Rue de Pommessargues, Montepellier Herault, 34000, FR

Mandatory US Agent: FDA Listing Inc.

## Products

Total registered: 1
Top product codes: DRX
Regulation §: 870.2360

Proprietary names: K-myo x1000 patches pack, K Myo x1000 patches pack, K Myo Accessories

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223016566173%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3016566173