Ansell Healthcare is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ansell Healthcare - FDA 510(k) Cleared Devices
Recent clearances: GAMMEX PI Hybrid Micro (340002055)
1
Total
1
Cleared
0
Denied
Ansell Healthcare has 1 FDA 510(k) cleared medical devices. Based in Reno, US.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ansell Healthcare Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ansell Healthcare
1 devices