Covalontechnologies, Inc.

Covalontechnologies, Inc. — FDA 510(k) Submissions

Covalontechnologies, Inc. has submitted 6 FDA 510(k) premarket notifications since 2005, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dressing, Wound, Drug, Drape, Surgical, Wound Dressing With Animal-derived Material(s), Catheter, Retention Type, Balloon . Use the specialty filter in the sidebar to narrow results.