Flexx Junior (FLX-J00, FLX-J50)
Nov 2025
250d
Karma Mobility Co, Ltd.
1
Total
1
Cleared
0
Denied
Karma Mobility Co, Ltd. — FDA 510(k) Submissions
Karma Mobility Co, Ltd. 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 Wheelchair, Mechanical . Use the specialty filter in the sidebar to narrow results.
1 devices