Schutz-Dental GmbH is one of 199 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Schutz-Dental GmbH - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Schutz-Dental GmbH has 6 FDA 510(k) cleared medical devices. Based in Rosbach, DE.
Historical record: 6 cleared submissions from 2005 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Schutz-Dental GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Schutz-Dental GmbH
6 devices
Cleared
Oct 24, 2016
Capo Hybrid, Capo Slow Flow, Capo Flow, Capo Natural, Capo Universal, Nano...
Dental
517d
Cleared
Feb 12, 2015
TIZIAN BLANK, TIZIAN ZIRCONIUM REINFORCED COMPOSITE BLANK, TIZIAN COLOR...
Dental
476d
Cleared
Aug 24, 2007
TIZIAN CERAMIC, FLOW, PLATE, FIX & ZR BLANKS
Dental
137d
Cleared
Oct 26, 2005
FUTURAPRESS LT, N AND HP, FUTURAJET, FUTURASELF, FUTURAGEN AND FUTURACRYL 2000
Dental
86d
Cleared
Oct 17, 2005
REVENEER CERAMIC REPAIR SYSTEM
Dental
67d
Cleared
Jun 29, 2005
SEBOND PINK LIGHT 5G, SEBOND PINK DARK 5G, SEBOND SMART 5ML, SEBOND GRIP 3G,...
Dental
65d