Stork Instrumente G M B H

FDA Filings

This page includes the latest FDA filings for Stork Instrumente 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 Number: 8010547
• FEI Number: 1000168975
• Name: Franz Menean
• Owner & Operator: STORK INSTRUMENTE GMBH
• Contact Address: ENGENERSTR. 29 --; EMMINGEN-LIPTINGEN 1 DE-BW Baden-Wurttemberg 78576 DE
• Official Correspondent:
  • FRANZ - MENEAN
  • 049-7465-825-x
• US Agent:
  • Franz Menean
  • MEDAGENT, Inc.
  • 603 5702039
  • 603 5702055
  • mail@medagent-usa.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 112 CORPORATE DR ; Portsmouth, NH 03801 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K030665 STORK INSTRUMENTE GMBH	BONE WIRE	2003-03-25