Dermawave, LLC is one of 25763 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dermawave, LLC - FDA 510(k) Cleared Devices
Recent clearances: DERMAWAVE 5000 COMBI MAX SYSTEM
1
Total
1
Cleared
0
Denied
Dermawave, LLC has 1 FDA 510(k) cleared medical devices. Based in Loxahatchee, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Dermawave, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Dermawave, LLC
1 devices