FDA.reportPublic FDA data

ROB LARSEN

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30044757543004475754ROB LARSEN1N2026-01-014628 WEST SKYHAWK DRIVE WEST JORDAN UT US 84084

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
584181648168058K254197Picasso Pro Diode Laser (002-00460)GEX2026-03-11
584182008720698K092616ASCENT BOND UNIVERSAL ADHESIVE SYSTEM, MODELS 006-00029, 006-00030, 006-00044, 006-00045KLE2009-10-21
584181102143950K091300ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079KLE2009-07-23
584181201343053K070070ASCENT DENTAL CLEANSERLBH2007-05-25
584182043446769K062886ASCENT PIT AND FISSURE SEALANT, MODEL 006-00019EBC2006-11-06
584181412118693
584181522141246
584182016335706

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KLE22009-10-21
LBH22007-05-25
GEX12026-03-11
EBC12006-11-06