Imbiotechnologies L T D

FDA Filings

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

FDA Registration(s)

• Registration Number: 3012120143
• FEI Number: 3012120143
• Name: IMBIOTECHNOLOGIES LTD
• Owner & Operator: IMBiotechnologies Ltd
• Contact Address: 9650 20th Avenue, NW Suite 215; Edmonton CA-AB Alberta T6N 1G1 CA
• Official Correspondent:
  • Michael Stewart
  • 1-780-9456609-x
• US Agent:
  • Gordon MacFarlane
  • ICONplc
  • 919 8738962
  • 215 6996288
  • Gordon.MacFarlane@iconplc.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 9650 20th Avenue, NW Suite 215; Edmonton Alberta, T6N 1G1 CA
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
GUDID 07540270000032 IMBiotechnologies Ltd	Occlusin 500	2019-05-30
GUDID 07540270000025 IMBiotechnologies Ltd	Occlusin 500	2019-05-30
GUDID 07540270000018 IMBiotechnologies Ltd	Occlusin 500	2019-05-30
GUDID 07540270000063 IMBiotechnologies Ltd	Occlusin 500	2019-02-25
GUDID 07540270000056 IMBiotechnologies Ltd	Occlusin 500	2019-02-25
GUDID 07540270000049 IMBiotechnologies Ltd	Occlusin 500	2019-02-25
GUDID 07540270000070 IMBiotechnologies Ltd	Occlusin 500	2018-11-22
PMN K093813 | KRD IMBIOTECHNOLOGIES LTD	Occlusin 500 Artificial Embolization Device	2016-05-01
PMN K093813 | KRD IMBIOTECHNOLOGIES LTD	Ekobi Embolization Microspheres	2016-05-01