Apyx Medical Corporation(Formerly Bovie 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(Formerly Bovie Medical Corporation) - FDA 51...
Recent clearances: Renuvion APR Handpiece, Renuvion Dermal Handpiece, Renuvion Dermal System, J-Plasma Precise FLEX Handpiece
4
Total
4
Cleared
0
Denied
Apyx Medical Corporation(Formerly Bovie Medical Corporation) has 4 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Last cleared in 2022. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Apyx Medical Corporation(Formerly Bovie Medical Corporation) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Apyx Medical Corporation (Formerly Bovie Medical Corporation as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Apyx Medical Corporation(Formerly Bovie Medical Corporation)
4 devices
Cleared
CT
Jul 15, 2022
Renuvion APR Handpiece
General & Plastic Surgery
102d
Cleared
CT
May 25, 2022
Renuvion Dermal Handpiece, Renuvion Dermal System
General & Plastic Surgery
362d
Cleared
Jan 04, 2021
J-Plasma Precise FLEX Handpiece
General & Plastic Surgery
98d
Cleared
Jul 30, 2019
Renuvion/J-Plasma Precise Handpiece
General & Plastic Surgery
56d