FDA.reportPublic FDA data

Longeviti Neuro Solutions

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30146807403014680740Longeviti Neuro Solutions1N2026-01-01101 W. Dickman St Suite 600 Baltimore MD US 21230

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2200991067674394K260709ClearFit Ti Ring 14mm (171750);ClearFit Ti Ring 14mm with Slot (171751);ClearFit Ti Ring 20mm (171752);ClearFit Ti Ring 20mm with Slot (171753);ClearFit Ti Ring 30mm (171754)GXN2026-06-25
2200991409033253K231920Longeviti ClearFit OTS Cranial ImplantGXN2023-11-09
2200991291167861K212058Longeviti ClearFit™ OTS Cranial ImplantsGXN2021-09-08
2200991735415877K211514Longeviti PorousFit implantKKY2021-07-15
2200991396346720K210616Longeviti PMMA Static Cranial ImplantGXN2021-03-31
2200991853919868K203349Longeviti ClearFit Cranial ImplantGXN2020-12-16
2200992030992645K202901Longeviti ClearFit Cranial ImplantGXN2020-10-30
2200991334464879K191210Longeviti ClearFit Cranial ImplantGXN2020-01-09
2200991910145932K170410Longeviti PMMA Static Cranial ImplantGXN2018-03-23
2200991107656240

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GXN82026-06-25
KKY12021-07-15