Integra Life Sciences is one of 20488 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integra Life Sciences - FDA 510(k) Cleared Devices
Recent clearances: DURAGEN SECURE DURAL REGNERATION MATRIX, INTEGRITY SPINAL CARE SYSTEM, ACCELL EVO3 (FORMERLY ACCELL A2I)
3
Total
3
Cleared
0
Denied
Integra Life Sciences has 3 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 3 cleared submissions from 2011 to 2012.
Browse the FDA 510(k) cleared devices submitted by Integra Life Sciences Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Integra Life Sciences
3 devices