Pressio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pressio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UNiTi ACDF Implant System
1
Total
1
Cleared
0
Denied
Pressio, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pressio, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Pressio, Inc.
1 devices