Medical Device Manufacturer · US , Washington , DC

Septodont - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2003

9

Total

9

Cleared

0

Denied

Septodont has 9 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2021. Active since 2003. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Septodont Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Septodont

9 devices

1-9 of 9

Cleared Sep 16, 2021

BioRoot Flow 0.5g, BioRoot Flow 2g

Cleared Aug 10, 2021

Biodentine XP 500, Biodentine XP 200

Cleared Feb 13, 2018

Cleared Jun 27, 2014

Cleared Feb 17, 2010

Cleared Oct 30, 2009

Cleared May 11, 2007

Cleared May 02, 2005

SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70

Cleared Nov 20, 2003

PLASTALGIN AND PLASTALGIN ORTHO