Spinendos G M B H

FDA Filings

This page includes the latest FDA filings for Spinendos 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: 3009499159
• FEI Number: 3009499159
• Name: Franz Menean
• Owner & Operator: Spinendos GmbH
• Contact Address: Wotanstrasse 119 ; Muenchen DE-BY Bayern 80639 DE
• Official Correspondent:
  • Thomas Chen
  • 49-89-45237322-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 Drive, Unit 12 Pease International Tradeport; Portsmouth, NH 03801 US
• Establishment Type:
  • Repack or Relabel Medical Device
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
FSM Franz Menean [Spinendos GmbH]	Instrument Tray	2018-05-16
PMN K130778 | HRX Franz Menean [Spinendos GmbH]	Discoscope	2014-04-17
PMN K130778 | HRX Franz Menean [Spinendos GmbH]	Cercival Endoscope	2014-04-17