# Sinexus, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: LYA (1)
- Predicates its devices cite: 4 (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 whose devices it cites most
- Synthemed Corp.: 1 (https://510kreport.com/company/synthemed)
- Carbylan Biosurgery: 1 (https://510kreport.com/company/carbylan-biosurgery)
- Polyganics B.V.,: 1 (https://510kreport.com/company/polyganics)
- Walter Lorenz Surgical, Inc.: 1 (https://510kreport.com/company/walter-lorenz-surgical)

## Firms that cite its devices most
- Sts Medical: 1 (https://510kreport.com/company/sts-medical)

## Its most-cited devices
- K092401: Sinexus Sinus Stent Gen 2, Model 1999-25 (2009), cited by 1

## Recent decisions
- K092401: Sinexus Sinus Stent Gen 2, Model 1999-25 (Nov 17, 2009)

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