FDA.reportPublic FDA data

Lumitex Medical Devices Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
10001228101000122810Lumitex Medical Devices Inc.1N2020-04-258300 Dow Circle Suite 400 Strongsville OH US 44136

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1266101644615812K120820GIRAFFE BLUE SPOT PT LITELBI2012-06-08
1266101988470536K053568BILISOFT PHOTOTHERAPY SYSTEMLBI2006-04-17
1266101004552605
1266101173006799
1266101289353158

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LBI22012-06-08