Vitrolife G M B H

FDA Filings

This page includes the latest FDA filings for Vitrolife 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: 3003843927
• FEI Number: 3003843927
• Name: Vitrolife GmbH
• Owner & Operator: Vitrolife GmbH
• Contact Address: DR.-PAULING-STR.9 --; BRUCKBERG DE-NOTA 84079 DE
• Official Correspondent:
  • SUSANNE - SCHWEITZER
  • 49-8765-939900-x
• US Agent:
  • DAVID HOPELY
  • NEXTGEN LIFELABS
  • 215 4101987 0
  • sue@nextgenlifelabs.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: DR.-PAULING-STR. 9 ; BRUCKBERG Bayern, 84079 DE
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K192008 | MRX Vitrolife GmbH	Octax NaviLase	2020-04-06
PMN K192008 | MRX Vitrolife GmbH	Octax LaserShotM	2020-04-06
PMN K192008 Vitrolife GmbH	LaserShot M, NaviLase	2020-03-25