Klingel Medical Metal G M B H

FDA Filings

This page includes the latest FDA filings for Klingel Medical Metal 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 Number3004370612
FEI Number3004370612
NameFranz Menean
Owner & OperatorKlingel medical metal GmbH
Contact AddressHanauer Str. 5-7
Pforzheim DE-BW Baden-Wurttemberg 75181 DE
Official Correspondent
  • Erwin Fredel
  • 049-7231-6519-50
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address112 CORPORATE DR
Portsmouth, NH 03801 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Franz Menean [Klingel medical metal GmbH]
Titanium scan body2012-11-26
Franz Menean [Klingel medical metal GmbH]
Titanium Base2011-04-04

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