Wieland Dental + Technik GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Wieland Dental + Technik GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Zenostar MT, Zenostar Color Liquids, IVOBASE CAD FOR ZENOTEC, IVOBASE CAD BOND, IVOBASE CAD MODELLING LIQUID, zenostar MO, Zenostar T, Zenostar VisualiZr
45
Total
45
Cleared
0
Denied
Wieland Dental + Technik GmbH & Co. KG has 45 FDA 510(k) cleared dental devices. Based in Pforzheim, DE.
Historical record: 45 cleared submissions from 2002 to 2015.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ivoclar Vivadent, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Wieland Dental + Technik GmbH & Co. KG
45 devices
Cleared
Dec 16, 2015
Zenostar MT, Zenostar Color Liquids
Dental
139d
Cleared
Aug 13, 2015
IVOBASE CAD FOR ZENOTEC, IVOBASE CAD BOND, IVOBASE CAD MODELLING LIQUID
Dental
106d
Cleared
Jan 05, 2015
zenostar MO, Zenostar T, Zenostar VisualiZr
Dental
145d
Cleared
May 24, 2013
ZENOLUX
Dental
119d
Cleared
Oct 17, 2011
ZENOTEC ZR BRIDGE, ZENOSTAR ZR TRANSLUCENT, ZENOTEC COLOR ZR, ZENOSTAR COLOR ZR
Dental
28d
Cleared
Mar 16, 2011
ZENOFLEX DIMENSION
Dental
79d
Cleared
Feb 16, 2011
ZENOSTAR MAGIC GLAZE
Dental
79d
Cleared
Sep 18, 2008
ZENO AI ECO DISC
Dental
41d
Cleared
Apr 08, 2008
ZENO PMMA DISC
Dental
74d
Cleared
Nov 21, 2007
ZENO ZR DISC
Dental
19d
Cleared
Apr 30, 2007
PRESSX ZR
Dental
40d
Cleared
Jul 22, 2005
ZIROX
Dental
67d
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