Medifun Corporation

Medifun Corporation — FDA 510(k) Submissions

Medifun Corporation has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Multiple Use Blood Lancet For Single Patient Use Only, Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature . Use the specialty filter in the sidebar to narrow results.