Ketonix Ab

FDA Filings

This page includes the latest FDA filings for Ketonix Ab. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011676007
FEI Number3011676007
NameKETONIX AB
Owner & OperatorKetonix AB
Contact AddressBorgasgatan 12
Varberg SE-N Hallands lan [SE-13] 43237 SE
Official Correspondent
  • Michel O Lundell
  • 46-705-195990-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressBorgasgatan 12
Varberg Hallands lan [SE-13], 43237 SE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
KETONIX AB
KETONIX2015-04-23

Related Finance Registrations
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.