Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Ocuject with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 25, 2024: LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Oct 25, 2024 | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety NeedleK242956 · QNS | 510(k) clearances |
| Nov 27, 2023 | SteriCap Safety Needle; VitreJect Safety NeedleK233343 · FMI | 510(k) clearances |
| Sep 14, 2023 | VitreJect® Needle; OcuSafe® NeedleK230959 · FMI | 510(k) clearances |
| Sep 8, 2023 | VitreJect SyringeK230372 · QLY | 510(k) clearances |
| Oct 13, 2021 | MiniLoad SyringeK212544 · FMF | 510(k) clearances |
| Sep 30, 2021 | SteriCap Mini Needle and Standard NeedlesK212805 · FMI | 510(k) clearances |
| Feb 19, 2021 | MiniLoad SyringeK202432 · FMF | 510(k) clearances |
| Jul 10, 2017 | Mini NeedleK170768 · FMI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
