Pression, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pression, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pression Wave PRO External Counter-Pulsation System
1
Total
1
Cleared
0
Denied
Pression, Inc. has 1 FDA 510(k) cleared medical devices. Based in Coatesville, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pression, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Broderick Regulatory Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pression, Inc.
1 devices