Ed. Geistlich Soehne AG Fuer Chemische Industrie is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ed. Geistlich Soehne AG Fuer Chemische Industrie - FDA 510(k) Cleared...
6
Total
6
Cleared
0
Denied
Ed. Geistlich Soehne AG Fuer Chemische Industrie has 6 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 6 cleared submissions from 2003 to 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ed. Geistlich Soehne AG Fuer Chemische Industrie Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ed. Geistlich Soehne AG Fuer Chemische Industrie
6 devices
Cleared
Mar 18, 2010
BIO-OSS COLLAGEN
Dental
223d
Cleared
May 30, 2008
MUCOGRAFT COLLAGEN MATRIX
Dental
151d
Cleared
Jun 06, 2006
MUCOGRAFT
Dental
34d
Cleared
Aug 09, 2005
BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE
Dental
168d
Cleared
Nov 15, 2004
BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE REGENERATION
Dental
94d
Cleared
Jan 24, 2003
MUCOGRAFT
Dental
543d