Toefx, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Toefx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hamilton, CA.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Toefx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Toefx, Inc.
1 devices