Difusion Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Difusion Technologies - FDA 510(k) Cleared Devices
Recent clearances: XIHPOS™ ZFUZE™ Interbody Fusion System
3
Total
3
Cleared
0
Denied
Difusion Technologies has 3 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 3 cleared submissions from 2010 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Difusion Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells as regulatory consultant.
FDA 510(k) Regulatory Record - Difusion Technologies
3 devices