# Sonoma Orthopedics Products, Inc.

- Location (FDA's records): Santa Rosa, CA
- FDA decisions: 2 (2015–2016): 2 510(k) clearances
- Product codes: HWC (1), HSB (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (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
- Acumed, LLC: 2 (https://510kreport.com/company/acumed)
- Syntec Scientific Corp.: 1 (https://510kreport.com/company/syntec-scientific)
- Sonoma Orthopedic Products, Inc.: 1 (https://510kreport.com/company/sonoma-orthopedic-products)

## Firms that cite its devices most
- Arthrex, Inc.: 2 (https://510kreport.com/company/arthrex)
- Intrafuse, LLC: 1 (https://510kreport.com/company/intrafuse)

## Its most-cited devices
- K160069: Sonoma Fibula Repair System (2016), cited by 3

## Recent decisions
- K160069: Sonoma Fibula Repair System (Mar 10, 2016)
- K150376: Sonoma Cancellous Bone Screw and Washer (Jun 12, 2015)

Source page: https://510kreport.com/company/sonoma-orthopedics-products