TFX-LT2000 Therapy Light
Nov 2022
570d
Toefx, Inc.
1
Total
1
Cleared
0
Denied
Toefx, Inc. — FDA 510(k) Submissions
Toefx, Inc. has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
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1 devices