Auragen Aesthetics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Auragen Aesthetics, LLC - FDA 510(k) Cleared Devices
Recent clearances: AuraGen 123 Suction Lipoplasty System (A123)
1
Total
1
Cleared
0
Denied
Auragen Aesthetics, LLC has 1 FDA 510(k) cleared medical devices. Based in Weston, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Auragen Aesthetics, 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 - Auragen Aesthetics, LLC
1 devices