Menicon B V

FDA Filings

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

FDA Registration(s)
Registration Number3003357577
FEI Number3003357577
NameMenicon B.V.
Owner & OperatorMENICON CO. LTD.
Contact Address21-19 AOI, 3-CHOME, NAKA-KU --
NAGOYA JP-23 Aiti 460-0006 JP
Official Correspondent
  • Tetsuji Kawai
  • 81-52-9351676-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressWaanderweg 6
Emmen Drenthe, 7812 HZ NL
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
Menicon B.V. [MENICON CO. LTD.]
Menicon Z Large Diameter2011-08-30
Menicon B.V. [MENICON CO. LTD.]
Menicon Z Irregular Cornea2008-10-31
Menicon B.V. [MENICON CO. LTD.]
Menicon Z DW2007-11-29

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