NanoPress 760A-BT (760A-BT)
Feb 2026
56d
Mego Afek , Ltd.
1
Total
1
Cleared
0
Denied
Mego Afek , Ltd. — FDA 510(k) Submissions
Mego Afek , Ltd. 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 Sleeve, Limb, Compressible . Use the specialty filter in the sidebar to narrow results.
1 devices