# OTTO BOCK ITALIA SRL

FEI: 3001917653
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Export Device to the United States But Perform No Other Operation on Device
Owner/operator: Ottobock SE & Co. KGaA (#8010097)

Address: VIA FILIPPO TURATI 5/7, BUDRIO Bologna, 40054, IT

Mandatory US Agent: Otto Bock HealthCare LP

## Products

Total registered: 1
Top product codes: IQE
Regulation §: 890.3490

Proprietary names: Lumbo Direxa High, Dorso Osteo Care Spinal Orthosis, Lumbo Direxa Stable, Spine Sport, Lumbo Sensa, Dorso Direxa Posture, Dorso Carezza Posture, Hyperextension brace, Lumbo Carezza, Dyneva light

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223001917653%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3001917653