# Oculinum, Inc.

- Location (FDA's records): Berkeley, CA
- FDA decisions: 3 (1986–1990): 3 510(k) clearances
- Product codes: HLW (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Technomed Europe: 1 (https://510kreport.com/company/technomed-europe)

## Its most-cited devices
- K900098: Monopolar Needle Electrode (1990), cited by 1

## Recent decisions
- K900279: Oculinum Injection Amplifier (Feb 9, 1990)
- K900098: Monopolar Needle Electrode (Feb 9, 1990)
- K854793: Monopolar Injection Needle Electrode (Feb 18, 1986)

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