Talladium, Inc. is one of 4760 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Talladium, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Talladium, Inc. has 7 FDA 510(k) cleared medical devices. Based in Valencia, US.
Historical record: 7 cleared submissions from 1989 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Talladium, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Talladium, Inc.
7 devices
Cleared
Sep 15, 2016
Luminesse Shaded Zirconia SZ
Dental
422d
Cleared
Oct 21, 2015
Luminesse Anterior Zirconia AT
Dental
89d
Cleared
Jun 15, 2015
LUMINESSE PRE-SINTERED ZIRCONIA COLORING LIQUID
Dental
230d
Cleared
Apr 24, 2015
Luminesse PMMA
Dental
242d
Cleared
Dec 17, 2014
LUMINESSE PORCELAIN SYSTEM
Dental
258d
Cleared
May 21, 2010
LUMINESSE ZR BLANKS
Dental
115d
Cleared
Dec 20, 1989
TALLADIUM TILITE CERAMIC ALLOY
Dental
195d