Lifecell Corporation
Lifecell Corporation appears in FDA public data with 0 recalls, 5 510(k) clearances, 11 FDA inspections, and 2 compliance actions on record. Its most recent 510(k) clearance was granted on May 28, 2020.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 11
- Compliance Actions
- 2
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K193539 | REVOLVE ENVI 600 Advanced Adipose System | May 28, 2020 |
| K163647 | Revolve Envi 600 Advanced Adipose System | August 25, 2017 |
| K162752 | ARTIA Reconstructive Tissue Matrix Perforated | February 24, 2017 |
| K150712 | LTM-Perforated Surgical Mesh | July 2, 2015 |
| K142326 | HP Tissue Matrix | December 23, 2014 |