CIONIC NEURAL SLEEVE (NS-200)
May 2025
140d
Cionic, Inc.
1
Total
1
Cleared
0
Denied
Cionic, Inc. — FDA 510(k) Submissions
Cionic, Inc. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Stimulator, Neuromuscular, External Functional . Use the specialty filter in the sidebar to narrow results.
1 devices