# RUNLITE S.A.

FEI: 6347
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: RUNLITE SA (#8020160)

Address: 9 AVENUE DE LA COOPERATION, MICHEROUX, SOUMAGNE Liege, 4630, BE

Mandatory US Agent: Kinetec USA, Inc.

## Products

Total registered: 1
Top product codes: FYH
Regulation §: 878.3910

Proprietary names: X-Lite, 3D-Lite

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%226347%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=6347