Jeneric Ind.

Jeneric Ind. — FDA 510(k) Submissions

Jeneric Ind. has submitted 25 FDA 510(k) premarket notifications since 1982, of which 25 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Alloy, Metal, Base, Alloy, Other Noble Metal, Alloy, Gold-based Noble Metal, Powder, Porcelain, Alloy, Amalgam . Use the specialty filter in the sidebar to narrow results.