Dura Tap, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dura Tap, LLC - FDA 510(k) Cleared Devices
Recent clearances: Gazelle Polypropylene Suture and Delivery Device, Gazelle PTFE and Suture Delivery Device
2
Total
2
Cleared
0
Denied
Dura Tap, LLC has 2 FDA 510(k) cleared medical devices. Based in Wayne, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dura Tap, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ambriel Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dura Tap, LLC
2 devices