Encora X1
Feb 2026
265d
Encora, Inc.
1
Total
1
Cleared
0
Denied
Encora, Inc. — FDA 510(k) Submissions
Encora, Inc. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include External Upper Limb Tremor Stimulator . Use the specialty filter in the sidebar to narrow results.
1 devices