Rob Larsen

FDA Filings

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

FDA Registration(s)
Registration Number3004475754
FEI Number3004475754
NameROB LARSEN
Owner & OperatorCAO Group, Inc.
Contact Address4628 West Skyhawk Drive
West Jordan UT 84084 US
Official Correspondent
  • Robert Larsen
  • x-801-4955503-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4628 WEST SKYHAWK DRIVE
WEST JORDAN, UT 84084 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
ROB LARSEN [CAO Group, Inc.]
Visco Tip2018-09-14
ROB LARSEN [CAO Group, Inc.]
Liqua Tip2018-09-14
ROB LARSEN [CAO Group, Inc.]
FE Scrub Tip2018-09-14
ROB LARSEN [CAO Group, Inc.]
BlissEtch2009-12-22
ROB LARSEN [CAO Group, Inc.]
BlissBond2009-12-22
ROB LARSEN [CAO Group, Inc.]
BlissEtch2009-12-22
ROB LARSEN [CAO Group, Inc.]
BlissBond2009-12-22
ROB LARSEN [CAO Group, Inc.]
FastFix2009-12-22
ROB LARSEN [CAO Group, Inc.]
CleanPrep2007-11-07
ROB LARSEN [CAO Group, Inc.]
FISSURE SEALANT2007-03-27
ROB LARSEN [CAO Group, Inc.]
Ascent Seal Pit & Fissure Sealant2007-03-27
ROB LARSEN [CAO Group, Inc.]
ASCENT PIT2007-03-27
ROB LARSEN [CAO Group, Inc.]
DIRECT VU ELLIPTICAL BIOPSY PUNCH2004-03-02
ROB LARSEN [CAO Group, Inc.]
DIRECT VU ELLIPTICAL BIOPSY PUNCH2004-03-02

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