Carl Zeiss Meditec Cataract Technology Inc

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30121230333012123033Carl Zeiss Meditec Cataract Technology Inc1N2026-01-018740 Technology Way Reno NV US 89521

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2267081457791533K243395MICOR 700 with Auto I/AHQC2025-08-08
2267081044858502K222236miCOR System Lens Fragmentation SystemHQC2022-08-24
2267081184735412K214028MICOR Lens Fragmentation SystemHQC2022-09-09
2267081120004045K200584xPORT 304 (miCOR) System Lens Fragmentation SystemHQC2020-07-31
2267081532988927

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HQC42025-08-08

PMN#