# KINOVA

FEI: 3009538853
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Kinova (#10045047)

Address: 4333 Grande-Allee, Boisbriand Quebec, J7H 1M7, CA

Mandatory US Agent: Partners in Medicine LLC

## Products

Total registered: 1
Top product codes: KNO
Regulation §: 890.3910

Proprietary names: Kinova Lift Arm

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009538853%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009538853