# Sinusys Corporation

- Location (FDA's records): Orinda, CA
- FDA decisions: 2 (2013–2016): 2 510(k) clearances
- Product codes: LRC (2)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (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
- Entellus Medical, Inc.: 2 (https://510kreport.com/company/entellus-medical)
- Acclarent, Inc.: 1 (https://510kreport.com/company/acclarent)
- Entrigue Surgical, Inc.: 1 (https://510kreport.com/company/entrigue-surgical)

## Recent decisions
- K160770: Vent-Os Sinus Dilation family (Jun 29, 2016)
- K133016: Vent-OS Sinus Dilation System (Dec 9, 2013)

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