Endo Twinn B.V. is one of 150 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Endo Twinn B.V. - FDA 510(k) Cleared Devices
Recent clearances: DOWN PAK, ENDO TWINN
2
Total
2
Cleared
0
Denied
Endo Twinn B.V. has 2 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.
Historical record: 2 cleared submissions from 2005 to 2007. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Endo Twinn B.V. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kema Quality B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Endo Twinn B.V.
2 devices