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
1931737801
Device Listing 1931737801
Listing Summary
#
Listing key
1931737801
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
23143
3004704697
3004704697
Jon Ward
1
N
2026-01-01
11705 Boyette Road #503 Riverview FL US 33569