Rti Biologics, Inc. is one of 19585 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rti Biologics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FORTIVA PORCINE DERMIS, TUTOPATCH, TUTOMESH, MODELS 68350, 68351, 68352, 68353, 68354, 68355, 68356, 68357, 68358, TUTOPATCH, TUTOMESH
3
Total
3
Cleared
0
Denied
Rti Biologics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Alachua, US.
Historical record: 3 cleared submissions from 2008 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Rti Biologics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rti Biologics, Inc.
3 devices