Emergo Europe Consulting is one of 143 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Emergo Europe Consulting - FDA 510(k) Cleared Devices
Recent clearances: Ceramill Zolid FX
1
Total
1
Cleared
0
Denied
Emergo Europe Consulting has 1 FDA 510(k) cleared medical devices. Based in The Hague, NL.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Emergo Europe Consulting Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Emergo Europe Consulting
1 devices