Dentaurum is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentaurum - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Dentaurum has 7 FDA 510(k) cleared medical devices. Based in Newtown, US.
Historical record: 7 cleared submissions from 2003 to 2006. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentaurum Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dentaurum
7 devices
Cleared
Nov 09, 2006
TOMAS PIN SD 6, 8, AND 10 MM
Dental
57d
Cleared
Oct 25, 2006
TOMAS PIN 6 MM
Dental
42d
Cleared
Nov 21, 2003
CONTEC DUO, CONTEC LC, CONTEC LCR
Dental
266d
Cleared
Oct 07, 2003
DENTAURUM GLASTEC DENTAL ORTHODONTIC CEMENT
Dental
81d
Cleared
Aug 25, 2003
DENTAURUM MIX TWO-PASTE BRACKET ADHESIVE
Dental
150d
Cleared
Aug 25, 2003
DENTAURUM NO-MIX ONE STEP BRACKET ADHESIVE
Dental
150d
Cleared
Jun 10, 2003
CONTEC LIGHT
Dental
102d