# Apyx Medical Corporation (Formerly Bovie Medical Corporation)

- Location (FDA's records): Clearwater, FL
- FDA decisions: 4 (2019–2022): 4 510(k) clearances
- Names in FDA's records: Apyx Medical Corporation(Formerly Bovie Medical Corporation) (2); Apyx Medical Corporation (Formerly Bovie Medical Corporation (2)
- Product codes: GEI (4)
- 510(k) review time since 2016: median 100 days, against 148 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bovie Medical Corporation: 3 (https://510kreport.com/company/bovie-medical)
- Energist, Ltd.: 1 (https://510kreport.com/company/energist)
- Bovie Medical Corporation Dba Apyx Medical Corporation: 1 (https://510kreport.com/company/bovie-medical-dba-apyx-medical)

## Firms that cite its devices most
- Apyx Medical Corporation: 2 (https://510kreport.com/company/apyx-medical)

## Its most-cited devices
- K220970: Renuvion APR Handpiece (2022), cited by 2

## Recent decisions
- K220970: Renuvion APR Handpiece (Jul 15, 2022)
- K211652: Renuvion Dermal Handpiece, Renuvion Dermal System (May 25, 2022)
- K202880: J-Plasma Precise FLEX Handpiece (Jan 4, 2021)
- K191484: Renuvion/J-Plasma Precise Handpiece (Jul 30, 2019)

Source page: https://510kreport.com/company/apyx-medical-formerly-bovie-medical