Pixxgen Corporation is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Pixxgen Corporation - FDA 510(k) Cleared Devices
Recent clearances: Prudent 1717, Prudent 1417, Prudent 1212, Pixx2430 Digital Diagnostic X-Ray Receptor Panel, PIXX 1717
4
Total
4
Cleared
0
Denied
Pixxgen Corporation has 4 FDA 510(k) cleared medical devices. Based in Anyang-Si, KR.
Last cleared in 2021. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Pixxgen Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Pixxgen Corporation
4 devices