Cartessa Aesthetics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cartessa Aesthetics - FDA 510(k) Cleared Devices
Recent clearances: SubNovii Advanced Plasma Technology
1
Total
1
Cleared
0
Denied
Cartessa Aesthetics has 1 FDA 510(k) cleared medical devices. Based in Melville, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cartessa Aesthetics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hoy and Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Cartessa Aesthetics
1 devices