Printbio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Printbio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 3DMatrix DynaFlex (DynaFlex), 3DMatrix Surgical Mesh
2
Total
2
Cleared
0
Denied
Printbio, Inc. has 2 FDA 510(k) cleared medical devices. Based in Long Island City, US.
Latest FDA clearance: May 2025. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Printbio, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Printbio, Inc.
2 devices