Medical Device Manufacturer · NL , Amsterdam

Endo Twinn B.V. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Total

Cleared

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.

Endo Twinn B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Endo Twinn B.V.

2 devices

1-2 of 2