Ceremed , Inc. is one of 4755 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ceremed , Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Ceremed , Inc. has 20 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 20 cleared submissions from 2004 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ceremed , Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ceremed , Inc.
20 devices
Cleared
Sep 27, 2016
Biopor Porous Polyethylene Implants
Neurology
125d
Cleared
Jul 14, 2016
Biopor, AOC Porous Polyethylene, Cerepor
General & Plastic Surgery
97d
Cleared
Apr 16, 2015
BIOPOR AOC POROUS POLYETHYLENE, CEREPOR
General & Plastic Surgery
279d
Cleared
Sep 12, 2013
ADAPTAIN, ADAPTAIN FASTWRAP, ENVELOCK, BIOWAI
Ear, Nose, Throat
58d
Cleared
Nov 27, 2012
ADAPTAIN FASTWRAP, ENVELOCK, GRAFTAIN
Ear, Nose, Throat
97d
Cleared
Jun 06, 2012
ADAPTAIN SOLUBLE IMPLANT MATERIAL
Ear, Nose, Throat
133d
Cleared
Jan 05, 2011
CERETENE SOLUBLE IMPLANT MATERIAL
Ear, Nose, Throat
82d
Cleared
Oct 08, 2010
OSTENE CT, AOC CT, OSTEOTENE, CERETENE
General & Plastic Surgery
77d
Cleared
Jun 22, 2009
OSTENE CT, AOC CT, OSTEOTENE, CERETENE
General & Plastic Surgery
18d
Cleared
Sep 24, 2008
OSTENE CT SOLUBLE BONE HEMOSTASIS IMPLANT MATERIAL, AOC CT, AOC, OSTENE,...
General & Plastic Surgery
27d
Cleared
Sep 18, 2008
AOC, OSTENE, AOC IMPLANT MATERIAL, CERETENE, OSTENE LUBE, AOC-LV
Ear, Nose, Throat
42d
Cleared
Jul 18, 2008
AOC SOLUBLE IMPLANT MATERIAL
Ear, Nose, Throat
46d