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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