# Ocujet, LLC

- Location (FDA's records): Newport Beach, CA
- FDA decisions: 2 (2015–2019): 2 510(k) clearances
- Product codes: FMI (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tsk Laboratory, Japan: 1 (https://510kreport.com/company/tsk-laboratory-japan)
- Ocuject, LLC: 1 (https://510kreport.com/company/ocuject)

## Firms that cite its devices most
- Ocuject, LLC: 2 (https://510kreport.com/company/ocuject)

## Its most-cited devices
- K151571: Mini Needle (2015), cited by 1
- K183016: SteriCap Mini Needle (2019), cited by 1

## Recent decisions
- K183016: SteriCap Mini Needle (May 7, 2019)
- K151571: Mini Needle (Oct 14, 2015)

Source page: https://510kreport.com/company/ocujet