FDA.reportPublic FDA data

DILON TECHNOLOGIES INC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
11256123002931663DILON TECHNOLOGIES INC1Y2026-01-01701 Mariners Row, Suite 200 NEWPORT NEWS VA US 23606

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
556411948261031P170012HEMOBLAST™ BellowsPMX2017-12-15
556411269866976K984466DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5IYX1999-03-16
556411955124281K110384DILON 6800 ACELLA (ACELLA)IYX2011-05-03
556411369483519K082588GAMMALOC SYSTEM, MODEL 03-00001IYX2009-12-11
556411237176541
556411288881464

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IYX32011-05-03
PMX12017-12-15