Genteel, LLC is one of 13040 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genteel, LLC - FDA 510(k) Cleared Devices
Recent clearances: Genteel Lancing Device
1
Total
1
Cleared
0
Denied
Genteel, LLC has 1 FDA 510(k) cleared medical devices. Based in Midland, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Genteel, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Genteel, LLC
1 devices