Wieland Dental + Technik GmbH & Co. KG

Wieland Dental + Technik GmbH & Co. KG — FDA 510(k) Submissions

Wieland Dental + Technik GmbH & Co. KG has submitted 45 FDA 510(k) premarket notifications since 2002, of which 45 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Alloy, Gold-based Noble Metal, Powder, Porcelain, Alloy, Other Noble Metal, Cement, Dental, Crown And Bridge, Temporary, Resin . Use the specialty filter in the sidebar to narrow results.