FDA 510(k) Applications Submitted by NEOSS LTD

FDA 510(k) Number Submission Date Device Name Applicant
K090452 02/23/2009 NEOSS IMPLANT SYSTEM 03.25 NEOSS LTD
K113376 11/16/2011 NEOSS PROACTIVE TAPERED IMPLANT NEOSS LTD
K071838 07/05/2007 NEOSS VARIOUS TITANIUM ABUTMENTS NEOSS LTD
K150669 03/16/2015 Neoss TiBase, Neoss CoCr Abutments (Mono and Multi) Neoss Ltd
K143327 11/20/2014 Neoss Ti Reinforced Membrane Neoss Ltd
K043195 11/18/2004 NEO IMPLANT SYSTEM NEOSS LTD
K211396 05/05/2021 Neoss Individual Prosthetics Neoss Ltd


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