Piccolo Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Piccolo Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PM2™ System with ECGuide™ Connector, PM2+ System and SmartPICC Stylet, PM2 System and ECGuide Connector
4
Total
4
Cleared
0
Denied
Piccolo Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Nov 2025. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Piccolo Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Arina Consulting and RQM+.
FDA 510(k) Regulatory Record - Piccolo Medical, Inc.
4 devices