Longeviti Neuro Solutions, LLC

Longeviti Neuro Solutions, LLC — FDA 510(k) Submissions

Longeviti Neuro Solutions, LLC has submitted 8 FDA 510(k) premarket notifications since 2018, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Cranioplasty, Preformed, Non-alterable, Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction . Use the specialty filter in the sidebar to narrow results.