Orthomod, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Orthomod, LLC has 1 FDA 510(k) cleared medical devices. Based in Dayton, US.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthomod, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Technologies as regulatory consultant.
1 devices