Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1868883339
Device Listing 1868883339
Listing Summary
#
Listing key
1868883339
Premarket submission
K231387
Device
Endofill
Applicant
Lumendo AG
Product code
KIF
Decision date
2023-07-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
325306
3030405669
3030405669
Andreas Schmocker
1
N
2026-01-01
123 Linden Blvd Apt 17j Brooklyn NY US 11226