Vinyl Technology, Inc.

Vinyl Technology, Inc. — FDA 510(k) Submissions

Vinyl Technology, Inc. has submitted 5 FDA 510(k) premarket notifications since 1987, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Splint, Extremity, Inflatable, External, Trousers, Anti-shock . Use the specialty filter in the sidebar to narrow results.