Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO is one of 219 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO - FDA 510(k) Clear...
4
Total
4
Cleared
0
Denied
Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO has 4 FDA 510(k) cleared medical devices. Based in Bremen, DE.
Historical record: 4 cleared submissions from 1998 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO Filter by specialty or product code using the sidebar.
Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO — FDA 510(k) Products and Clearance History
4 devices
Cleared
Nov 12, 2013
BECE CAD ZIRKON HT+
Dental
127d
Cleared
Mar 14, 2013
BEGOPAL+
Dental
84d
Cleared
Jul 06, 2009
BECE PRESS
Dental
137d
Cleared
Oct 28, 1998
BEGOPAL 300
Dental
56d