FDA.reportPublic FDA data

THE LINDEN GROUP CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30123364613012336461THE LINDEN GROUP CORP.1N2026-01-012B Wing Dr Cedar Knolls NJ US 07927

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1918612066791660K191705OptikView GUP2103CMIPGY2020-03-16
1918611680967505K152847DIVA ZSP5812CMI with QUBYX PerfectLum bundlePGY2015-11-17
1918611052206158
1918611406319717
1918611540040386

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PGY22020-03-16

PMN#