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Neoss, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K211396Neoss Individual ProstheticsMay 17, 2022
K150669Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)October 8, 2015
K143327Neoss Ti Reinforced MembraneApril 13, 2015
K113376NEOSS PROACTIVE TAPERED IMPLANTSeptember 5, 2012
K090452NEOSS IMPLANT SYSTEM 03.25May 22, 2009
K081851NEOSS ACCESS ABUTMENTSMarch 2, 2009
K083561NEOSS PROACTIVE IMPLANTFebruary 11, 2009
K071838NEOSS VARIOUS TITANIUM ABUTMENTSOctober 19, 2007
K043195NEO IMPLANT SYSTEMMarch 7, 2005