Ocuject, LLC

8 FDA 510(k) medical device clearances.

Top product codes for Ocuject, LLC

Recent clearances by Ocuject, LLC

K242956 — LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle QNS · 2024-10-25
K233343 — SteriCap Safety Needle; VitreJect Safety Needle FMI · 2023-11-27
K230959 — VitreJect® Needle; OcuSafe® Needle FMI · 2023-09-14
K230372 — VitreJect Syringe QLY · 2023-09-08
K212544 — MiniLoad Syringe FMF · 2021-10-13
K212805 — SteriCap Mini Needle and Standard Needles FMI · 2021-09-30
K202432 — MiniLoad Syringe FMF · 2021-02-19
K170768 — Mini Needle FMI · 2017-07-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.