Kreyenberg G M B H

FDA Filings

This page includes the latest FDA filings for Kreyenberg 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 Number3009455196
FEI Number3009455196
NameKREYENBERG GMBH
Owner & OperatorKreyenberg GmbH
Contact AddressOststrasse 51
Norderstedt DE-SH Schleswig-Holstein D-22844 DE
Official Correspondent
  • Dominik Wiese
  • 49-040-5219670-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressOststrasse 51
Norderstedt Schleswig-Holstein, D-22844 DE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
KREYENBERG GMBH
T2 Flexible Nail2013-06-20
KREYENBERG GMBH
SPEEDLOCK SLEEVE 2002013-06-20
KREYENBERG GMBH
SPEEDLOCK SLEEVE 1802013-06-20
KREYENBERG GMBH
SPEEDLOCK SLEEVE 1702013-06-20

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.