Metalor Dental USA Corp.

Metalor Dental USA Corp. — FDA 510(k) Submissions

Metalor Dental USA Corp. has submitted 67 FDA 510(k) premarket notifications since 1991, of which 67 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, Attachment, Precision, All, Implant, Endosseous, Root-form, Alloy, Metal, Base . Use the specialty filter in the sidebar to narrow results.