Orthofix Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthofix Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Reef TO/TA System
1
Total
1
Cleared
0
Denied
Orthofix Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lewisville, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthofix Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Orthofix Medical, Inc.
1 devices