Medical Device Manufacturer · US , Claremont , NH

Plastiflex Group NV - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

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.

FDA 510(k) Regulatory Record - Plastiflex Group NV

2 devices

1-2 of 2