Koninklijke (Royal) Utermohlen is one of 61 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Koninklijke (Royal) Utermohlen - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Koninklijke (Royal) Utermohlen has 1 FDA 510(k) cleared medical devices. Based in Wolvega, NL.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Koninklijke (Royal) Utermohlen Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Koninklijke (Royal) Utermohlen
1 devices