Xod, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Xod, Inc. has 1 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Latest FDA clearance: Feb 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Xod, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Xod, Inc.
1 devices