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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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