FDA 510(k) Applications Submitted by JENNIFER M. JACKSON

FDA 510(k) Number Submission Date Device Name Applicant
K132219 07/17/2013 STRAUMANN(R) VARIOBASE(TM) ABUTMENT NNC, STRAUMANN(R) VARIOBASE(TM) ABUTMENT RN, STRAUMANN(R) VARIOBASE(TM) ABUTMENT WN, STRAUMANN USA, LLC
K192401 09/03/2019 Straumann Screw-Retained Abutments Straumann USA, LLC
K130222 01/29/2013 STRAUMANN DENTAL IMPLANT SYSTEM STRAUMANN USA, LLC
K123784 12/10/2012 STRAUMANN DENTAL IMPLANT SYSTEM STRAUMANN USA, LLC
K171784 06/15/2017 Straumann Dental Implant System Straumann USA, LLC
K142890 10/03/2014 Straumann Variobase Abutment NNC, Straumann Variobase Abutment RN, Straumann Variobase Abutment WN, Straumann Variobase Abutment NC, Straumann Variobase Abutment RC, IPS e.max CAD MO Coping, IPS e.max CAD LT Crown, IPS e.max CAD HT Crown, coron CoCr Singl STRAUMANN USA, LLC
K162890 10/17/2016 BLT 02.9mm SC, SLA or SLActive, RXD, Loxim, SC Closure Cap and Healing Abutments, SC Temporary Abutments, SC Variobase Abutments, SC CARES Abutment STRAUMANN USA, LLC


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