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
1223535688
Device Listing 1223535688
Listing Summary
#
Listing key
1223535688
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
20365
9710644
3003949221
Rob Yamashita
1
N
2026-01-01
2710 Northridge Dr NW STE A Grand Rapids MI US 49544