Michaelk Hieda

FDA Filings

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

FDA Registration(s)

• Registration Number: 9616990
• FEI Number: 3008918179
• Name: MICHAELK.HIEDA
• Owner & Operator: NEMOTO KYORINDO CO., LTD.
• Contact Address: 2-27-20 HONGO (HONGO CTR. BLDG. 3RD FLOOR); BUNKYO-KU JP-13 Tokyo 113-0033 JP
• Official Correspondent:
  • JIM E KNIPFER
  • 813-584-28571-x
• US Agent:
  • MICHAELK.HIEDA
  • NEMOTO MEDICAL U.S., INC.
  • 949 6326183 0
  • 949 6438989
  • mkh@nemotous.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 24992 DEL MONTE ST. ; LAGUNA HILLS, CA 92653 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K173450 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	PRESS DUO elite	2018-02-21
PMN K173450 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	PRESS DUO elite AG	2018-02-21
PMN K133189 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	alpha 7	2014-07-28
PMN K133189 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	Dual Shot alpha 7	2014-07-28
PMN K133189 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	DSA7	2014-07-28
PMN K092896 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	Rempress	2012-10-04
PMN K092896 | DXT MICHAELK.HIEDA [NEMOTO KYORINDO CO., LTD.]	Rempress Angiographic Injection System	2012-10-04

Similar & Related FDA Registered Companies

• NEMOTO MEDICAL U.S., INC.