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 Number: 3012478173
• FEI Number: 3012478173
• Name: OCUJECT, LLC
• Owner & Operator: OcuJect, LLC
• Contact Address: 1441 Avocado Avenue, Suite 204 ; Newport Beach CA 92660 US
• Official Correspondent:
  • Laurence Harvey
  • x-858-6758200-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 13240 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	Device	Date
GUDID 00855265008434 Ocuject, LLC	VitreJect Syringe	2023-09-18
GUDID 00855265008403 Ocuject, LLC	VitreJect Syringe	2023-09-18
GUDID 00850040387926 Ocuject, LLC	VitreJect Syringe	2023-09-18
GUDID 00850047046277 Ocuject, LLC	MiniLoad Syringe	2023-09-08
GUDID 00850047046246 Ocuject, LLC	MiniLoad Syringe	2023-09-08
GUDID 00850047046154 Ocuject, LLC	MiniLoad Syringe	2023-09-08
GUDID 00850047046123 Ocuject, LLC	MiniLoad Syringe	2023-09-08
GUDID 00850040387247 Ocuject, LLC	MiniLoad Syringe	2023-09-08
PMN K212544 OcuJect, LLC	MiniLoad Syringe	2021-10-13
PMN K212805 OcuJect, LLC	SteriCap Mini Needle And Standard Needles	2021-09-30
PMN K202432 OcuJect, LLC	MiniLoad Syringe	2021-02-19
PMN K183016 | FMI OCUJECT, LLC	SteriCap Mini Needle	2019-12-17
PMN K170768 | FMI OCUJECT, LLC	Mini Needle	2017-09-01
PMN K170768 OcuJect, LLC	Mini Needle	2017-07-10