Engineered Tissue Solutions, LLC is one of 19478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Engineered Tissue Solutions, LLC - FDA 510(k) Cleared Devices
Recent clearances: Mirragen Advanced Wound Matrix, 4x4”, Mirragen Advanced Wound Matrix, 2x2”, Mirragen Advanced Wound Matrix, 1x6”
1
Total
1
Cleared
0
Denied
Engineered Tissue Solutions, LLC has 1 FDA 510(k) cleared medical devices. Based in Rolla, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Engineered Tissue Solutions, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Engineered Tissue Solutions, LLC
1 devices