Lifecell Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Lifecell Corp. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Washington, US.
Historical record: 10 cleared submissions from 2005 to 2013.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
10 devices
Cleared
Apr 17, 2013
LTN - LAPAROSCOPIC SURGICAL MESH
General & Plastic Surgery
23d
Cleared
Aug 10, 2012
LIFECELL TISSUE EXPANDER
General & Plastic Surgery
344d
Cleared
Aug 03, 2012
LTM-LABAROSCOPIC SURGICAL MESH
General & Plastic Surgery
95d
Cleared
Nov 14, 2008
LTM-BPS SURGICAL MESH
General & Plastic Surgery
105d
Cleared
Oct 08, 2008
LTM WOUND DRESSING
General & Plastic Surgery
75d
Cleared
Apr 03, 2008
LTM-T SURGICAL MESH
General & Plastic Surgery
52d
Cleared
Oct 19, 2007
LTM-RC SURGICAL MESH
General & Plastic Surgery
91d
Cleared
Jun 11, 2007
LRTM SURGICAL MESH
General & Plastic Surgery
104d
Cleared
Jan 03, 2007
LIFECELL DURAL SUBSTITUTE MATRIX
Neurology
247d
Cleared
Dec 28, 2005
ALLOCRAFT DBM
Orthopedic
89d