Medical Device Manufacturer · CA , Dundas

Koninklijke Utermohlen NV - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Koninklijke Utermohlen NV has 2 FDA 510(k) cleared medical devices. Based in Dundas, CA.

Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Koninklijke Utermohlen NV Filter by specialty or product code using the sidebar.

Koninklijke Utermohlen NV is one of 209 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Koninklijke Utermohlen NV

2 devices

1-2 of 2