Knittel Glaeser

FDA Filings

This page includes the latest FDA filings for Knittel Glaeser. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 1000469910
• FEI Number: 1000469910
• Name: Waldemar Knittel Glasbearbeitungs GmbH
• Owner & Operator: KNITTEL GLAESER
• Contact Address: VARRENTRAPPSTRASSE 3 --; BRAUNSCHWEIG, NIEDERSACHSEN DE-NOTA 38114 DE
• Official Correspondent:
  • Fabio - Insalata
  • 49-531-59000038-x
• US Agent:
  • Dale Charles
  • Leica Biosystems
  • 815 6782000 6162
  • 815 6786044
  • Dale.Charles@Leicabiosystems.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: VARRENTRAPPSTRASSE 5 ; BRAUNSCHWEIG, NIEDERSACHSEN Niedersachse, 38114 DE
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
KES Waldemar Knittel Glasbearbeitungs GmbH [KNITTEL GLAESER]	Starfrost	2011-08-01
KES Waldemar Knittel Glasbearbeitungs GmbH [KNITTEL GLAESER]	CellSolutions Glass Slides	2011-08-01