Curasan AG is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curasan AG - FDA 510(k) Cleared Devices
Recent clearances: Ceracell Ortho Foam, Cerasorb Ortho Foam, CURASAN OSSEOLIVE DENTAL
10
Total
10
Cleared
0
Denied
Curasan AG has 10 FDA 510(k) cleared medical devices. Based in Garner,, US.
Historical record: 10 cleared submissions from 2002 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Curasan AG Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Yes Medical Device Services GmbH and PaxMed International, LLC.
FDA 510(k) Regulatory Record - Curasan AG
10 devices
Cleared
Sep 17, 2018
Ceracell Ortho Foam
Orthopedic
80d
Cleared
Dec 02, 2016
Cerasorb Ortho Foam
Orthopedic
277d
Cleared
Dec 20, 2012
CURASAN OSSEOLIVE DENTAL
Dental
610d
Cleared
Mar 10, 2011
CERACELL DENTAL
Dental
80d
Cleared
Jan 12, 2011
OSBONE DENTAL
Dental
104d
Cleared
Aug 19, 2010
BONEOPTIMIZER
Orthopedic
147d
Cleared
Jun 11, 2007
REVOIS IMPLANT SYSTEM
Dental
243d
Cleared
Mar 26, 2004
CERASORB M ORTHO
Orthopedic
56d
Cleared
Aug 13, 2003
MODIFICATION TO CERASORB ORTHO
Orthopedic
77d
Cleared
Mar 18, 2002
CERASORB ORTHO
Orthopedic
89d