Meta Systems Co., Ltd.

Meta Systems Co., Ltd. — FDA 510(k) Submissions

Meta Systems Co., Ltd. has submitted 4 FDA 510(k) premarket notifications since 2016, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Handpiece, Direct Drive, Ac-powered, Locator, Root Apex, Activator, Ultraviolet, For Polymerization . Use the specialty filter in the sidebar to narrow results.