ZenTite (Unicorn+); ZenTite (Unicorn+I); ZenTite (Unicorn+II); ZenTite (Unicorn+III)
Jan 2026
30d
Shenzhen Peninsula Medical Group
1
Total
1
Cleared
0
Denied
Shenzhen Peninsula Medical Group — FDA 510(k) Submissions
Shenzhen Peninsula Medical Group 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 Electrosurgical, Cutting & Coagulation & Accessories . Use the specialty filter in the sidebar to narrow results.
1 devices