Euroteknika is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Euroteknika - FDA 510(k) Cleared Devices
Recent clearances: iPhysio® System
3
Total
3
Cleared
0
Denied
Euroteknika has 3 FDA 510(k) cleared medical devices. Based in Montreal, Quebec, CA.
Latest FDA clearance: Mar 2025. Active since 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Euroteknika Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Euroteknika
3 devices