Iotron Industries Canada Inc

FDA Filings

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

FDA Registration(s)
Registration Number9680579
FEI Number1000203464
NameDavid Lennarz
Owner & OperatorIotron Industries Canada, Inc.
Contact Address1425 Kebet Way
Port Coquitlam CA-BC British Columbia V3C 6L3 CA
US Agent
Importing Logistics Registration
ImporterTenet Medical Engineering
Address203 11979- 40th Street SE
Calgarz, T2Z 4M3 CANADA
Email Addressbrent.king@smith-nephew.com
Phone1 403 5710750
Importer TypeSPECIFICATIONS DEVELOPER
SubdivisionCA-AB
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address144 Research Drive
HAMPTON, VA 23666 US
Establishment TypeSterilize Medical Device for Another Party (Contract Sterilizer)



FDA Filings

Device
Company
DeviceDate
David Lennarz [Iotron Industries Canada, Inc.]
Disposable Rigid Scope Introducer2013-04-12
David Lennarz [Iotron Industries Canada, Inc.]
Glue Seal 902012-11-27
David Lennarz [Iotron Industries Canada, Inc.]
WS Kit2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
SS Kit2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
LS Kit2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
ES Kit2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
Boot Liner2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
AS Kit2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
Switch Drape2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
Electric SS Kit2012-11-21
David Lennarz [Iotron Industries Canada, Inc.]
FAST1 Intraosseous Infusion System2007-12-20

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