Suretex Limited

Suretex Limited — FDA 510(k) Submissions

Suretex Limited has submitted 6 FDA 510(k) premarket notifications since 2022, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Condom, Condom, Synthetic, Lubricant, Personal . Use the specialty filter in the sidebar to narrow results.