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
1503246439
Device Listing 1503246439
Listing Summary
#
Listing key
1503246439
Premarket submission
K243765
Device
LuMon(TM) System
Applicant
Sentec AG
Product code
QEB
Decision date
2025-08-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
22988
3004149774
3004149774
Stephen Gorski
1
N
2026-01-01
S65w35739 Piper Rd Eagle WI US 53119