Lifecell Corporation

5 FDA 510(k) medical device clearances.

Top product codes for Lifecell Corporation

FTM — General, Plastic Surgery 3 devices
MUU — General, Plastic Surgery 2 devices

Recent clearances by Lifecell Corporation

K193539 — REVOLVE ENVI 600 Advanced Adipose System MUU · 2020-05-28
K163647 — Revolve Envi 600 Advanced Adipose System MUU · 2017-08-25
K162752 — ARTIA Reconstructive Tissue Matrix Perforated FTM · 2017-02-24
K150712 — LTM-Perforated Surgical Mesh FTM · 2015-07-02
K142326 — HP Tissue Matrix FTM · 2014-12-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.