FDA.reportPublic FDA data

NEUROPHET, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30256026183025602618NEUROPHET, INC.1N2026-01-0112F-15F, 314 Gangnam-daero, Gangnam-gu, Republic of Korea Seoul KR 06253

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3128921474352427K261273Neurophet AQUAQIH2026-05-15
3128921730065258K252563Neurophet SCALE PETQIH2026-05-15
3128921458204798K252496Neurophet AQUA AD PlusQIH2026-01-29
3128921623109235K242215Neurophet AQUA (V3.1)QIH2024-10-25
3128921058629889K221405Neurophet SCALE PETLLZ2022-08-05
3128921271442503K220437Neurophet AQUALLZ2023-05-10

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QIH42026-05-15
LLZ22023-05-10

PMN#