Medical Device Manufacturer · US , Newport Beach , CA

Ocuject, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2017

Recent clearances: LDS Needle, SteriCap Safety Needle, VitreJect® Needle

8
Total
8
Cleared
0
Denied

FDA 510(k) Regulatory Record - Ocuject, LLC General Hospital ✕

8 devices
1-8 of 8
Cleared Oct 25, 2024
LDS Needle
K242956 · QNS
General Hospital · 30d
Cleared Nov 27, 2023
SteriCap Safety Needle
K233343 · FMI
General Hospital · 59d
Cleared Sep 14, 2023
VitreJect® Needle
K230959 · FMI
General Hospital · 163d
Cleared Sep 08, 2023
VitreJect Syringe
K230372 · QLY
General Hospital · 207d
Cleared Oct 13, 2021
MiniLoad Syringe
K212544 · FMF
General Hospital · 62d
Cleared Sep 30, 2021
SteriCap Mini Needle and Standard Needles
K212805 · FMI
General Hospital · 28d
Cleared Feb 19, 2021
MiniLoad Syringe
K202432 · FMF
General Hospital · 178d
Cleared Jul 10, 2017
Mini Needle
K170768 · FMI
General Hospital · 118d
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