Plastiflex Group NV is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Plastiflex Group NV - FDA 510(k) Cleared Devices
Recent clearances: Hybernite RT, HYBERNITE RAINOUT CONTROL SYSTEM
2
Total
2
Cleared
0
Denied
Plastiflex Group NV has 2 FDA 510(k) cleared medical devices. Based in Claremont, US.
Historical record: 2 cleared submissions from 2010 to 2016. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Plastiflex Group NV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Plastiflex Group NV
2 devices