Syrma Johari Medtech Limited

Syrma Johari Medtech Limited — FDA 510(k) Submissions

Syrma Johari Medtech Limited 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, Muscle, Powered, For Muscle Conditioning . Use the specialty filter in the sidebar to narrow results.