Dyna-Med

Dyna-Med — FDA 510(k) Submissions

Dyna-Med has submitted 4 FDA 510(k) premarket notifications since 1976, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accessories, Traction, System, X-ray, Fluoroscopic, Image-intensified, Block, Bite . Use the specialty filter in the sidebar to narrow results.