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
1188954181
Device Listing 1188954181
Listing Summary
#
Listing key
1188954181
Premarket submission
K180947
Device
Orthopantomograph OP 3D
Applicant
Palodex Group OY
Product code
OAS
Decision date
2018-06-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
24549
3005383085
3005383085
Erika Martin
1
N
2026-01-01
450 Commerce Drive Quakertown PA US 18951