Invitron

FDA Filings

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

FDA Registration(s)

• Registration Number: 3005948789
• FEI Number: 3005948789
• Name: INVITRON
• Owner & Operator: Invitron
• Contact Address: Wyastone Business Park Wyastone Leys; Monmouth GB-MON Monmouthshire NP25 3SR GB
• US Agent:
  • David Lennarz
  • Registrar Corp
  • 757 2240177
  • 757 2240179
  • david.lennarz@registrarcorp.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Wyastone Business Park Wyastone Leys; Monmouth Monmouthshire, NP25 3SR GB
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
JKD INVITRON	IV2-104E C-Peptide ELISA	2008-12-23
JKD INVITRON	IV2-103E Total Proinsulin ELISA Kit	2008-12-23
JKD INVITRON	IV2-102E Intact Proinsulin ELSIA Kit	2008-12-23
JKD INVITRON	IV2-004 MLT C-Peptide Kit	2008-12-23
JKD INVITRON	IV2-003 MLT Total Proinsulin Kit	2008-12-23
JKD INVITRON	IV2-002 MLT Intact Proinsulin Kit	2008-12-23
CFP INVITRON	IV2-101E Insulin ELISA Kit	2008-12-23
CFP INVITRON	IV2-001 MLT Insulin Kit	2008-12-23