Lntegra Lifesciences is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lntegra Lifesciences - FDA 510(k) Cleared Devices
Recent clearances: Polydioxanone Surgical Scaffold
1
Total
1
Cleared
0
Denied
Lntegra Lifesciences has 1 FDA 510(k) cleared medical devices. Based in Princeton, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lntegra Lifesciences 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 - Lntegra Lifesciences
1 devices