# Kinetec SAS

FEI: 3006734242
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Kinetec USA, Inc. (#10045573)

Address: Zone Industrielle de Tournes, Rue Maurice Périn, Tournes Ardennes, F-08090, FR

Mandatory US Agent: Kinetec USA, Inc.

## Products

Total registered: 1
Top product codes: BXB
Regulation §: 890.5380

Proprietary names: Kinetec 6080, Kinetec USA, Kinetec Spectra XL, Kinetec Spectra, Kinetec Spectra Essential, Kinetec Prima Advance, Kinetec Prima XL, Kinetec Performa, Kinetec Centura B&W, Kinetec Breva

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006734242%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006734242