Company · US
Ocuject, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2024. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 25, 2024 | K242956 | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle Ocuject, LLC | QNS |
| Nov 27, 2023 | K233343 | SteriCap Safety Needle; VitreJect Safety Needle Ocuject, LLC | FMI |
| Sep 14, 2023 | K230959 | VitreJect® Needle; OcuSafe® Needle Ocuject, LLC | FMI |
| Sep 8, 2023 | K230372 | VitreJect Syringe Ocuject, LLC | QLY |
| Oct 13, 2021 | K212544 | MiniLoad Syringe Ocuject, LLC | FMF |
| Sep 30, 2021 | K212805 | SteriCap Mini Needle and Standard Needles Ocuject, LLC | FMI |
| Feb 19, 2021 | K202432 | MiniLoad Syringe Ocuject, LLC | FMF |
| Jul 10, 2017 | K170768 | Mini Needle Ocuject, LLC | FMI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||