Ontex Eeklo

FDA Filings

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

FDA Registration(s)
Registration Number3003449471
FEI Number3003449471
NameOntex Eeklo
Owner & OperatorOntex BVBA
Contact AddressKorte Keppestraat 21
Aalst BE-VOV Oost-Vlaanderen 9320 BE
Official Correspondent
  • Bart Waterschoot
  • 32-53-333649-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressKorte Moeie 53
Eeklo Oost-Vlaanderen, 9900 BE
Establishment TypeManufacture Medical Device




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