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
1005060891
Device Listing 1005060891
Listing Summary
#
Listing key
1005060891
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
78106
8021788
5682
Jon Ward
1
N
2026-01-01
11705 Boyette Road #503 Riverview FL US 33569