Tendonova Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Tendonova Corporation has 1 FDA 510(k) cleared medical devices. Based in Norcross, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tendonova Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tendonova Corporation
1 devices