Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Lifecell Corporation

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest Approval2020-05-28
TypeNumberDevice NameCodeDate
510(k) K193539 REVOLVE ENVI 600 Advanced Adipose System MUU 2020-05-28 View
510(k) K163647 Revolve Envi 600 Advanced Adipose System MUU 2017-08-25 View
510(k) K162752 ARTIA Reconstructive Tissue Matrix Perforated FTM 2017-02-24 View