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
1597009362
Device Listing 1597009362
Listing Summary
#
Listing key
1597009362
Premarket submission
K142358
Device
Osstell IDx
Applicant
Osstell AB
Product code
EKX
Decision date
2015-02-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
22451
3004070020
3004070020
OSSTELL AB
1
N
2026-01-01
Stampgaten 14 GOTEBORG Vastra Gotaland SE 41101