NOUVAG AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
NOUVAG AG - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
NOUVAG AG has 11 FDA 510(k) cleared dental devices. Based in Kaufbeuren, DE.
Historical record: 11 cleared submissions from 1996 to 2009.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - NOUVAG AG
11 devices
Cleared
Jun 29, 2009
MORCE POWER PLUS AND VARIOCARVE MORCELLATOR
Obstetrics & Gynecology
504d
Cleared
Aug 07, 2008
TCM ENDO 20
Dental
101d
Cleared
Nov 26, 2007
DISPENSER DP 20
General Hospital
168d
Cleared
Dec 22, 2004
TCM ENDO V, MODEL 1534
Dental
71d
Cleared
Dec 17, 2004
NOUVAG AG - VACUSON 40 AND VACUSON 60
General & Plastic Surgery
53d
Cleared
Nov 03, 2004
MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55
Dental
56d
Cleared
Oct 01, 2003
CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061,...
Dental
429d
Cleared
Nov 28, 2001
TCM ENDO III
Dental
65d
Cleared
May 11, 2000
MD 10, SEM, SM 12, CBM
Dental
70d
Cleared
Feb 09, 1999
TCM 3000 AND TCM ENDO
Dental
272d
Cleared
Jan 16, 1996
MICRO-DISPENSER 7000 & MICRODISPENSER 8000
Dental
95d