FDA.reportPublic FDA data

NEPTUNE MEDICAL, INC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30154518283015451828NEPTUNE MEDICAL, INC1N2026-01-011828 El Camino Real 5th Floor Burlingame CA US 94010

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2339701083287475K260503Triton 1 SystemFDF2026-09-03
2339701376021087K240853Pathfinder® CR SystemFED2024-06-27
2339701454926934K230801Pathfinder Endoscope Overtube with Balloon DeviceFED2023-07-28
2339701646118306K211301Pathfinder Endoscope OvertubeFED2021-05-28
2339702036278495K210915Pathfinder Endoscope CapFDS2021-05-25
2339701704707177K191415Pathfinder Endoscope OvertubeFED2019-08-30
2339701491952253

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FED42024-06-27
FDF12026-09-03
FDS12021-05-25