Kci USA, Inc. (Kinetic Concepts, Inc.) is one of 17415 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kci USA, Inc. (Kinetic Concepts, Inc.) - FDA 510(k) Cleared Devices
Recent clearances: V.A.C.ULTA Negative Pressure Wound Therapy System, PREVENA DUO, PREVENA PLUS DUO Incision Management Systems with PEEL & PLACE Dressings, V. A.C. VeraFlo Cleanse Choice Dressing System for use with the V.A.C. Ulta ...
Kci USA, Inc. (Kinetic Concepts, Inc.) has 13 FDA 510(k) cleared general & plastic surgery devices. Based in San Antonio, US.
Historical record: 13 cleared submissions from 2006 to 2017.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kci USA, Inc. as regulatory consultant.