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
2009159184
Device Listing 2009159184
Listing Summary
#
Listing key
2009159184
Premarket submission
K190812
Device
RAYSCAN a-Expert3D
Applicant
Ray Co., Ltd.
Product code
OAS
Decision date
2019-04-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
163009
3010445368
3010445368
JANGTAE (BRANDON) YOO
1
N
2026-01-01
400 Kelby Street, Ste 1500 Fort Lee NJ US 07024