Lifecell Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
11
Compliance Actions
2

Recent 510(k) Clearances

K-NumberDeviceDate
K193539REVOLVE ENVI 600 Advanced Adipose SystemMay 28, 2020
K163647Revolve Envi 600 Advanced Adipose SystemAugust 25, 2017
K162752ARTIA Reconstructive Tissue Matrix PerforatedFebruary 24, 2017
K150712LTM-Perforated Surgical MeshJuly 2, 2015
K142326HP Tissue MatrixDecember 23, 2014