Ocuject, LLC
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K242956 | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle | October 25, 2024 |
| K233343 | SteriCap Safety Needle; VitreJect Safety Needle | November 27, 2023 |
| K230959 | VitreJect® Needle; OcuSafe® Needle | September 14, 2023 |
| K230372 | VitreJect Syringe | September 8, 2023 |
| K212544 | MiniLoad Syringe | October 13, 2021 |
| K212805 | SteriCap Mini Needle and Standard Needles | September 30, 2021 |
| K202432 | MiniLoad Syringe | February 19, 2021 |
| K170768 | Mini Needle | July 10, 2017 |