FDA.reportPublic FDA data

Derek Wessman

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96114813002807220Derek Wessman1N2026-01-013300 N Triumph Blvd Ste 100 Lehi UT US 84043
96119173009431614Derek Wessman1N2026-01-013300 N Triumph Blvd Suite 100 Lehi UT US 84043
30057487843005748784Derek Wessman1N2026-01-013300 N Triumph Blvd Suite 100 Lehi UT US 84043
30429715063042971506Derek Wessman1N2026-01-013300 N Triumph Blvd Suite 100 Lehi UT US 84043

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
105941193290736K961152TUOHY EPIDURAL NEEDLESBSP1997-03-19
105941370037138K961151SPINAL NEEDLESBSP1997-03-19
413961965113653K191147OC-Auto SENSOR io iFOB TestOOX2020-01-02
413961637930159K143325OC-Light S FITKHE2015-08-20
413961923661176K092330OC-SENSOR DIANA IFOB TESTOOX2010-01-08
105941951198588K063380ECHOSTIM FACET TIPBSP2007-04-25
413961584674693K041408POLYMEDCO OC AUTO MICRO 80 FOB TESTOOX2004-10-21
413961858993393K041297POLYMEDCO OC LIGHT FOBT TESTKHE2004-08-12
105941187356591K030824LAP DISC 120 X 120MM X2CM, MODEL LD111, LAP DISC 120 X 120MMX 7CM,MODEL LD112GCJ2003-06-04
105941548031788K013109SONOPSYFCG2002-03-12
105942005189665K013108BIOSUCKNW2002-04-04
413961054061812
105941838253466
667801892031208
3460101909645959
667801979230566
105942016057187
105942059306151

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OOX32020-01-02
BSP32007-04-25
KHE22015-08-20
GCJ12003-06-04
KNW12002-04-04
FCG12002-03-12