Lifecell Corporation - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Lifecell Corporation has 5 FDA 510(k) cleared medical devices. Based in Branchburg, US.
Historical record: 5 cleared submissions from 2014 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lifecell Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Lifecell Corporation
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