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
1802126750
Device Listing 1802126750
Listing Summary
#
Listing key
1802126750
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
55170
2031637
3004474407
FZIOMED, INC.
1
N
2026-01-01
231 BONETTI DR San Luis Obispo CA US 93401