Menicon Co L T D Seki Plant

FDA Filings

This page includes the latest FDA filings for Menicon Co L T D Seki Plant. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3002807570
• FEI Number: 3002807570
• Name: Menicon Co., Ltd., Seki Plant
• Owner & Operator: MENICON CO. LTD.
• Contact Address: 21-19 AOI, 3-CHOME, NAKA-KU --; NAGOYA JP-23 Aiti 460-0006 JP
• Official Correspondent:
  • Tetsuji Kawai
  • 81-52-9351676-x
• US Agent:
  • Kurtis Brown
  • MENICON AMERICA, INC.
  • 781 6092042
  • 781 3735216
  • kurtis_brown@menicon.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 3, Shinhasama --; Seki Gihu, 501-3923 JP
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K180004 | LPL Menicon Co., Ltd., Seki Plant [MENICON CO. LTD.]	Miru 1month Menicon (1Month SiHy)	2018-02-23