FDA 510(k) Applications Submitted by KETTENBACH GMBH & CO KG
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K122039 |
07/11/2012 |
KINGSCROSS PL-C+B-10, KINGSCROSS PL-C+B-12, KINGSCROSS PL-C+B-08, KINGSCROSS B |
KETTENBACH GMBH & CO KG |
| K143104 |
10/29/2014 |
Visalys Core, Visalys PL-Core, Visalys PL-Core-C, Visalys PL-Core-X |
KETTENBACH GMBH & CO KG |
| K083701 |
12/15/2008 |
PANASIL INITIAL CONTACT AND PANASIL TRAY |
KETTENBACH GMBH & CO KG |
| K081120 |
04/21/2008 |
FUTAR (FUTAR, FUTAR D, FUTAR D FAST, FUTAR D SLOW, FUTAR SCAN BITE REGISTRATION MATERIALS |
KETTENBACH GMBH & CO KG |
| K082157 |
07/31/2008 |
KETTOSIL AND SILGINAT |
KETTENBACH GMBH & CO KG |
| K082560 |
09/04/2008 |
PANASIL IMPRESSION MATERIALS, INCLUDING PUTTY, BINETICS, TRAY, MONOPHASE AND CONTACT |
KETTENBACH GMBH & CO KG |
| K092867 |
09/18/2009 |
IDENTIUM HEAVY, MEDIUM, MEDIUM SOFT, LIGHT |
KETTENBACH GMBH & CO KG |
| K113279 |
11/07/2011 |
IDENTIUM HEAVY, IDENTIUM MEDIUM, IDENTIUM SCAN HEAVY, IDENTIUM SCAN MEDIUM, IDENTIUM SCAN LIGHT |
KETTENBACH GMBH & CO KG |
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