Kci USA, Inc. - FDA 510(k) Cleared Devices
28
Total
27
Cleared
1
Denied
Kci USA, Inc. has 27 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Latest FDA clearance: May 2024. Active since 2006.
Browse the FDA 510(k) cleared devices submitted by Kci USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kci USA, Inc.
1 devices