Ocuject, LLC
Ocuject, LLC holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2024.
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
- K233343 — SteriCap Safety Needle; VitreJect Safety Needle
- K230959 — VitreJect® Needle; OcuSafe® Needle
- K230372 — VitreJect Syringe
- K212544 — MiniLoad Syringe
- K212805 — SteriCap Mini Needle and Standard Needles
- K202432 — MiniLoad Syringe
- K170768 — Mini Needle
Data sourced from openFDA. This site is unofficial and independent of the FDA.