Lifecell Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
1
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K130817LTN - LAPAROSCOPIC SURGICAL MESHApril 17, 2013
K112534LIFECELL TISSUE EXPANDERAugust 10, 2012
K121289LTM-LABAROSCOPIC SURGICAL MESHAugust 3, 2012
K082176LTM-BPS SURGICAL MESHNovember 14, 2008
K082103LTM WOUND DRESSINGOctober 8, 2008
K080353LTM-T SURGICAL MESHApril 3, 2008
K071986LTM-RC SURGICAL MESHOctober 19, 2007
K070560LRTM SURGICAL MESHJune 11, 2007
K061208LIFECELL DURAL SUBSTITUTE MATRIXJanuary 3, 2007
K052735ALLOCRAFT DBMDecember 28, 2005