Ocuject L L C

FDA Filings

This page includes the latest FDA filings for Ocuject L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3012478173
FEI Number3012478173
NameOCUJECT, LLC
Owner & OperatorOcuJect, LLC
Contact Address1441 Avocado Avenue, Suite 204
Newport Beach CA 92660 US
Official Correspondent
  • Laurence Harvey
  • x-858-6758200-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address13240 Evening Creek Dr S Ste 304
San Diego, CA 92128 US
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
Ocuject, LLC
 VitreJect Ophthalmic Needle 2025-03-10
Ocuject, LLC
 VitreJect Ophthalmic Needle 2025-03-10
Ocuject, LLC
 VitreJect Ophthalmic Needle 2025-03-10
Ocuject, LLC
 VitreJect Ophthalmic Needle 2025-03-10
Ocuject, LLC
 VitreJect-DL Ophthalmic Needle 2025-03-10
Ocuject, LLC
 VitreJect Ophthalmic Syringe 2025-03-10
Ocuject, LLC
 VitreJect Ophthalmic Syringe 2025-03-10
Ocuject, LLC
 VitreJect Syringe 2023-09-18
Ocuject, LLC
 VitreJect Syringe 2023-09-18
Ocuject, LLC
 VitreJect Syringe 2023-09-18
Ocuject, LLC
 MiniLoad Syringe 2023-09-08
Ocuject, LLC
 MiniLoad Syringe 2023-09-08
Ocuject, LLC
 MiniLoad Syringe 2023-09-08
Ocuject, LLC
 MiniLoad Syringe 2023-09-08
Ocuject, LLC
 MiniLoad Syringe 2023-09-08
OcuJect, LLC
MiniLoad Syringe2021-10-13
OcuJect, LLC
SteriCap Mini Needle And Standard Needles2021-09-30
OcuJect, LLC
MiniLoad Syringe2021-02-19
OCUJECT, LLC
SteriCap Mini Needle2019-12-17
OCUJECT, LLC
Mini Needle2017-09-01
OcuJect, LLC
Mini Needle2017-07-10

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