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Company-Registration
1894517041
Device Listing 1894517041
Listing Summary
#
Listing key
1894517041
Premarket submission
K230959
Device
VitreJect® Needle; OcuSafe® Needle
Applicant
Ocuject, LLC
Product code
FMI
Decision date
2023-09-14
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