Tissue Regeneration Technologies

Tissue Regeneration Technologies — FDA 510(k) Submissions

Tissue Regeneration Technologies has submitted 2 FDA 510(k) premarket notifications since 2018, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Massager, Therapeutic, Electric, Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers . Use the specialty filter in the sidebar to narrow results.