Epflex Feinwerktechnik G M B H

FDA Filings

This page includes the latest FDA filings for Epflex Feinwerktechnik 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 Number3003289691
FEI Number3003289691
NameFranz Menean
Owner & OperatorEPFLEX FEINWERKTECHNIK GMBH
Contact AddressIM SCHWOELLBOGEN 24 --
DETTINGEN/ERMS DE-BW Baden-Wurttemberg D 72581 DE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address112 CORPORATE DR
Portsmouth, NH 03801 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device

FDA Filings

Device
Company
DeviceDate
EPflex Feinwerktechnik GmbH.
 Domia Front DOF2082021-08-02
EPflex Feinwerktechnik GmbH.
 Domia Front DOF2012021-08-02
EPflex Feinwerktechnik GmbH.
 Domia Front DOF1582021-08-02
EPflex Feinwerktechnik GmbH.
 Domia Front DOF1512021-08-02

Related Finance Registrations
NCAGE CodeCM108EPFLEX FEINWERKTECHNIK GMBH
CAGE CodeCM108EPFLEX FEINWERKTECHNIK GMBH
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