FDA.reportPublic FDA data

MAXIFLEX, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30068122153006812215MAXIFLEX, LLC1N2020-04-25512 Verret St New Orleans LA US 70114

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
729181739495200K111480MAXIFLEX - SEMI FLEX SCOPE, 25 TO 65 CMFGB2012-04-04
729182040213356K062725MAXIFLEX-SEMI FLEX SCOPEFGB2006-09-29
729181773915333K013300MAXIFLEX FIBER OPTIC ENERGY DELIVERY SYSTEMGEX2002-04-16

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FGB22012-04-04
GEX12002-04-16

GUDID#

73 records. Showing 1-40. Next