Greten Prismaflex G M B H

FDA Filings

This page includes the latest FDA filings for Greten Prismaflex 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: 3005687704
• FEI Number: 3005687704
• Name: Greten PRISMAFLEX GmbH
• Owner & Operator: OPTIKER GRETEN FOLIENOPTIK
• Contact Address: DOBBENWEG 3 --; BREMEN DE-NOTA 28203 DE
• US Agent:
  • JOHANT.W.VAN DALEN
  • Optego
  • 520 6174490 7001
  • 520 2091586
  • achirco@optego.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: DOBBENWEG 3 ; BREMEN Bremen, 28203 DE
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
HKT Greten PRISMAFLEX GmbH [OPTIKER GRETEN FOLIENOPTIK]	PRISM	2006-04-14
HKT Greten PRISMAFLEX GmbH [OPTIKER GRETEN FOLIENOPTIK]	FRESNEL	2006-04-14