Argen Precious Metals, Inc.

Argen Precious Metals, Inc. — FDA 510(k) Submissions

Argen Precious Metals, Inc. has submitted 217 FDA 510(k) premarket notifications since 1989, of which 217 received clearance as substantially equivalent to a predicate device.

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