Ocuject, LLC
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories4
Latest Approval2024-10-25
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K242956 | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle | QNS | 2024-10-25 | View |
| 510(k) | K233343 | SteriCap Safety Needle; VitreJect Safety Needle | FMI | 2023-11-27 | View |
| 510(k) | K230959 | VitreJect® Needle; OcuSafe® Needle | FMI | 2023-09-14 | View |
| 510(k) | K230372 | VitreJect Syringe | QLY | 2023-09-08 | View |
| 510(k) | K212544 | MiniLoad Syringe | FMF | 2021-10-13 | View |
| 510(k) | K212805 | SteriCap Mini Needle and Standard Needles | FMI | 2021-09-30 | View |
| 510(k) | K202432 | MiniLoad Syringe | FMF | 2021-02-19 | View |
| 510(k) | K170768 | Mini Needle | FMI | 2017-07-10 | View |
No matching devices.