Apyx Medical Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apyx Medical Corporation - FDA 510(k) Cleared Devices
Recent clearances: AYON Body Contouring System™ (AYON SYSTEM), AYON Body Contouring System (AYON SYSTEM), Renuvion® Micro Handpiece
6
Total
6
Cleared
0
Denied
Apyx Medical Corporation has 6 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Latest FDA clearance: May 2026. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Apyx Medical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Apyx Medical Corporation
6 devices
Cleared
May 08, 2026
AYON Body Contouring System™ (AYON SYSTEM)
General & Plastic Surgery
220d
Cleared
May 12, 2025
AYON Body Contouring System (AYON SYSTEM)
General & Plastic Surgery
132d
Cleared
Jun 09, 2023
Renuvion® Micro Handpiece
General & Plastic Surgery
99d
Cleared
Apr 27, 2023
Renuvion® APR Handpiece
General & Plastic Surgery
86d
Cleared
Feb 23, 2023
Renuvion® APR Handpiece
General & Plastic Surgery
122d
Cleared
Oct 11, 2022
Apyx One Console
General & Plastic Surgery
110d