Toefx, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Toefx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TFX-LT2000 Therapy Light
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.
510(k) submissions have been managed by Braunsolutions Regulatory Group as regulatory consultant.
FDA 510(k) Regulatory Record - Toefx, Inc.
1 devices