Vita Zahnfabrik H.Rauter GmbH & Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vita Zahnfabrik H.Rauter GmbH & Co. - FDA 510(k) Cleared Devices
Recent clearances: VITA YZ Multi Translucent, VITA YZ ST and VITA YZ XT
8
Total
8
Cleared
0
Denied
Vita Zahnfabrik H.Rauter GmbH & Co. has 8 FDA 510(k) cleared medical devices. Based in Brea, US.
Latest FDA clearance: Feb 2025. Active since 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Vita Zahnfabrik H.Rauter GmbH & Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vita North America as regulatory consultant.
FDA 510(k) Regulatory Record - Vita Zahnfabrik H.Rauter GmbH & Co.
8 devices
Cleared
Feb 21, 2025
VITA YZ Multi Translucent
Dental
63d
Cleared
Aug 01, 2018
VITA YZ ST and VITA YZ XT
Dental
135d
Cleared
Jun 30, 2016
VITA ENAMIC Implant Solutions (IS)
Dental
192d
Cleared
Dec 30, 2015
VITA VM LC Flow
Dental
131d
Cleared
Jan 31, 2014
VITA SUPRINITY(R)
Dental
212d
Cleared
Dec 13, 2012
ENAMIC
Dental
136d
Cleared
Aug 11, 2010
VITABLOCS
Dental
13d
Cleared
Mar 31, 2009
VITABLOCS, MODEL VX55-****
Dental
21d