Ximedica - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ximedica has 2 FDA 510(k) cleared medical devices. Based in Providence, US.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ximedica Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Veranex, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ximedica
2 devices