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
2014103801
Device Listing 2014103801
Listing Summary
#
Listing key
2014103801
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
44419
1063481
3001451326
Artivion, Inc.
1
Y
2026-01-01
1655 Roberts Blvd NW Kennesaw GA US 30144