Xeridiem Medical Devices, A Spectrum Plastics Group Company

Xeridiem Medical Devices, A Spectrum Plastics Group Company — FDA 510(k) Submissions

Xeridiem Medical Devices, A Spectrum Plastics Group Company has submitted 2 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gastrointestinal Tubes With Enteral Specific Connectors . Use the specialty filter in the sidebar to narrow results.