Koninklijke Utermohlen NV is one of 201 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Koninklijke Utermohlen NV - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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 — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jun 05, 2013
WART FREEZE
General & Plastic Surgery
90d
Cleared
Jun 23, 2011
WART FREEZE
General & Plastic Surgery
435d