FDA.reportPublic FDA data

DYNAREX CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
24310142431014DYNAREX CORP.1Y2027-01-0111 Dynarex Drive Middletown NY US 10941

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
370971321410163K172266Dynarex Three-Way StopcockFMG2018-03-14
370971158353783K152970Dynarex Xeroform Petrolatum DressingFRO2016-10-03
370971916275593K151575Dynarex Eye CupsLXQ2015-09-01
370971448850672K082863DYNAREX ENTERAL DELIVERY PUMP SET WITH SPIKE (1000ML), DYNAREX ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE (1000ML)KNT2009-01-09
370971176375539K081569DYNAREX/TILLOTSON NON-STERILE POWDER FREE BLUE NITRILE PATIENT EXAM GLOVE FOR USE WITH CHEMOTHERAPY DRUGSLZA2008-09-12
370971333137195K052743DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921CBP2005-12-22
370971498558905K012816DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414FRO2002-10-17

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FRO22016-10-03
FMG12018-03-14
LXQ12015-09-01
KNT12009-01-09
LZA12008-09-12
CBP12005-12-22

PMN#