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
1350448814
Device Listing 1350448814
Listing Summary
#
Listing key
1350448814
Premarket submission
K170768
Device
Mini Needle
Applicant
Ocuject, LLC
Product code
FMI
Decision date
2017-07-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
192299
3012478173
3012478173
OCUJECT, LLC
1
Y
2026-01-01
13240 Evening Creek Dr S Ste 304 San Diego CA US 92128