# INTENSIV SA

FEI: 1000225541
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Intensiv SA (#9001345)

Address: Via al Molino 107, Collina d'Oro / Montagnola Ticino, 6926, CH

Mandatory US Agent: REGISTRAR CORP

## Products

Total registered: 1
Top product codes: EHM
Regulation §: 872.6010

Proprietary names: Intensiv Bevelshape, Intensiv ApproxOpener, Intensiv Ortho-Strips Opener, Intensiv Proxoshape, Intensiv Proxoshape Flexible, Intensiv Proxoshape Coarse, Intensiv ProxoStrip Anterior, Intensiv ProxoStrip, Intensiv Ortho-Strips Coarse, Intensiv ProxoPolish

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221000225541%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1000225541