Condor Medtec G M B H

FDA Filings

This page includes the latest FDA filings for Condor Medtec G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009936738
FEI Number3009936738
NameFranz Menean
Owner & OperatorCondor MedTec GmbH
Contact AddressDr.-Krismann-Str. 15
Salzkotten DE-NW Nordrhein-Westfalen 33154 DE
Official Correspondent
  • Heidi Brautmeier
  • 049-5258-9916-0
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address112, Corporate Drive, Unit 1
Portsmouth, NH 03801 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Franz Menean [Condor MedTec GmbH]
RotexTable by Condor?2014-07-14
Franz Menean [Condor MedTec GmbH]
RotexShoe by Condor?2014-07-14

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