Kenneth Blake

FDA Filings

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

FDA Registration(s)
Registration Number3013784566
FEI Number3013784566
NameKenneth Blake
Owner & OperatorBerger Surgical Medical Products GmbH
Contact AddressKirchstrasse 22
Tuttlingen DE-BW Baden-Wurttemberg 78532 DE
Official Correspondent
  • Marcel J Hruby
  • 49-7461-9696-17
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address292 East Lafayette Frontage Road
Saint Paul, MN 55107 US
Establishment Type
  • Remanufacture Medical Device
  • Manufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Kenneth Blake [Berger Surgical Medical Products GmbH]
Septal Hook, 3 prong, 7mm hook, angled up and ot the side2020-02-10
Kenneth Blake [Berger Surgical Medical Products GmbH]
Septal Hook, 3 prong, 13 mm hook, angled up and ot the side2020-02-10
Kenneth Blake [Berger Surgical Medical Products GmbH]
Septal Hook, 3 prong, 10 mm hook, angled up and ot the side2020-02-10
Kenneth Blake [Berger Surgical Medical Products GmbH]
De Bakey Forceps titanium, 240 mm length2020-02-10
Kenneth Blake [Berger Surgical Medical Products GmbH]
De Bakey Forceps titanium, 195 mm length2020-02-10
Kenneth Blake [Berger Surgical Medical Products GmbH]
Septal Hook - Retractor2017-09-26
Kenneth Blake [Berger Surgical Medical Products GmbH]
LOFTUS 2-Level ACDF Distractor2017-09-26

Similar & Related FDA Registered Companies

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