Instylla, Inc.

Instylla, Inc. — FDA 510(k) Submissions

Instylla, Inc. has submitted 9 FDA 510(k) premarket notifications since 2019, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Syringe, Piston, Catheter, Continuous Flush, Device, Vascular, For Promoting Embolization . Use the specialty filter in the sidebar to narrow results.