Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Apyx Medical Corporation (Formerly Bovie Medical Corporation

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest Approval2022-05-25
TypeNumberDevice NameCodeDate
510(k) K211652 Renuvion Dermal Handpiece, Renuvion Dermal System GEI 2022-05-25 View
510(k) K202880 J-Plasma Precise FLEX Handpiece GEI 2021-01-04 View
↑