Sonoma Orthopedics Products, Inc. is one of 18469 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonoma Orthopedics Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Sonoma Fibula Repair System, Sonoma Cancellous Bone Screw and Washer
2
Total
2
Cleared
0
Denied
Sonoma Orthopedics Products, Inc. has 2 FDA 510(k) cleared medical devices. Based in Santa Rosa, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sonoma Orthopedics Products, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Memphis Regulatory Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sonoma Orthopedics Products, Inc.
2 devices