# ECHOSENS

FEI: 3010258456
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Echosens (#10043955)

Address: 6 rue Ferrus, Paris, 75014, FR

Mandatory US Agent: Echosens North America

## Products

Total registered: 2
Top product codes: ITX, IYO
Regulation §: 892.1570, 892.1560

Proprietary names: FibroScan 502 Touch, FibroScan, XL+ probe, M+ probe

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010258456%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010258456