Medical Device Manufacturer · US , Washington , DC

Neoss, Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2005

Recent clearances: Neoss Individual Prosthetics, Neoss TiBase, Neoss CoCr Abutments (Mono and Multi), Neoss Ti Reinforced Membrane

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neoss, Ltd. Dental ✕

9 devices

1-9 of 9

Cleared May 17, 2022

Neoss Individual Prosthetics

Cleared Oct 08, 2015

Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)

Cleared Apr 13, 2015

Neoss Ti Reinforced Membrane

Cleared Sep 05, 2012

NEOSS PROACTIVE TAPERED IMPLANT

Cleared May 22, 2009

NEOSS IMPLANT SYSTEM 03.25

Cleared Mar 02, 2009

NEOSS ACCESS ABUTMENTS

Cleared Feb 11, 2009

NEOSS PROACTIVE IMPLANT

Cleared Oct 19, 2007

NEOSS VARIOUS TITANIUM ABUTMENTS

Cleared Mar 07, 2005

NEO IMPLANT SYSTEM

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 18, 2026