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
1968846979
Device Listing 1968846979
Listing Summary
#
Listing key
1968846979
Premarket submission
K203290
Device
Bonelogic
Applicant
Disior, Ltd.
Product code
LLZ
Decision date
2021-02-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
288164
3018064242
3018064242
DISIOR OY
1
N
2026-01-01
HTC Helsinki, Building Pinta, Tammasaarenkatu 3 Helsinki Uusimaa FI 00180