FDA.reportPublic FDA data

IMEX

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30301515843030151584IMEX, LLC1N2026-01-0111820 West Market Place Suite K Fulton MD US 20759

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3237121674683664K982635CAREDOP IIJAF1998-08-07
3237121663666676K961250DYNATRON 125 ULTRASOUNDIMI1996-08-26
3237121586306988K942441IMEXDOP CT+JAF1994-08-23
3237121489912220K901593IMEX DOP-TONE IIKNG1990-07-02
3237121031547662K132057DYNATRON PELTIER THERMOSTIM PROBEGXY2014-01-24
3237121580445008K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEILY2012-02-09
3237121510921199K031329DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)IMI2003-10-22
3237121274319391

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IMI22003-10-22
JAF21998-08-07
GXY12014-01-24
ILY12012-02-09
KNG11990-07-02

PMN#

GUDID#