Optiker Greten Folienoptik

FDA Filings

This page includes the latest FDA filings for Optiker Greten Folienoptik. 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