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
1700955742
Device Listing 1700955742
Listing Summary
#
Listing key
1700955742
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
67432
3005984081
3005984081
LUMIQUICK DIAGNOSTICS, INC.
1
Y
2026-01-01
2946 SCOTT BLVD. SANTA CLARA CA US 95054