Lifecell Corporation - FDA 510(k) Cleared Devices
Recent clearances: REVOLVE ENVI 600 Advanced Adipose System, Revolve Envi 600 Advanced Adipose System, ARTIA Reconstructive Tissue Matrix Perforated
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Lifecell Corporation General & Plastic Surgery ✕
5 devices
Cleared
May 28, 2020
REVOLVE ENVI 600 Advanced Adipose System
General & Plastic Surgery
160d
Cleared
Aug 25, 2017
Revolve Envi 600 Advanced Adipose System
General & Plastic Surgery
245d
Cleared
Feb 24, 2017
ARTIA Reconstructive Tissue Matrix Perforated
General & Plastic Surgery
147d
Cleared
Jul 02, 2015
LTM-Perforated Surgical Mesh
General & Plastic Surgery
105d
Cleared
Dec 23, 2014
HP Tissue Matrix
General & Plastic Surgery
125d