Wefis G M B H

FDA Filings

This page includes the latest FDA filings for Wefis 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: 3006050792
• FEI Number: 3006050792
• Name: Jessica Dearth
• Owner & Operator: Wefis GmbH
• Contact Address: Konrad-Adenauer-Strasse 25 ; K?ln DE-NW Nordrhein-Westfalen 50996 DE
• Official Correspondent:
  • Juergen Nachbaur
  • 49-162-2356301-x
• US Agent:
  • Jessica Dearth
  • Dutch Ophthalmic, USA
  • 603 7538824
  • mcarignan@micro-vision.net
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 10, Continental Drive, Building one ; Exeter, NH 03833 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K190875 | HQC Jessica Dearth [Wefis GmbH]	Sure Touch Phaco Handpiece	2019-10-10