Excera Orthopedics, Inc. is one of 18555 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Excera Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FitRite™ Total Hip Arthroplasty System, EXCERA FITRITE TOTAL HIP ARTHROPLASTY SYSTEM
2
Total
2
Cleared
0
Denied
Excera Orthopedics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Shelton, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Excera Orthopedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Orchid Design as regulatory consultant.
FDA 510(k) Regulatory Record - Excera Orthopedics, Inc.
2 devices