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
1943635789
Device Listing 1943635789
Listing Summary
#
Listing key
1943635789
Premarket submission
K223841
Device
KBA3D
Applicant
S.M.A.I.O
Product code
LLZ
Decision date
2023-05-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
279474
3015383864
3015383864
S.M.A.I.O
1
N
2026-01-01
2 Place Berthe Morisot Parc Technologique SAINT-PRIEST Auvergne-Rhone-Alpes FR 69800