Printbio, Inc.

Printbio, Inc. — FDA 510(k) Submissions

Printbio, Inc. has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Absorbable, Plastic And Reconstructive Surgery . Use the specialty filter in the sidebar to narrow results.