# Apyx Medical Corporation

- Location (FDA's records): Clearwater, FL
- FDA decisions: 7 (2022–2026): 7 510(k) clearances
- Product codes: GEI (4), QPB (3)
- 510(k) review time since 2016: median 105 days, against 127 for FDA's reviews in the same codes and years (5 of 6 faster)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 4 (3 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
- Apyx Medical Corporation (Formerly Bovie Medical Corporation): 2 (https://510kreport.com/company/apyx-medical-formerly-bovie-medical)
- Microaire Surgical Instruments, LLC: 2 (https://510kreport.com/company/microaire-surgical-instruments)
- Bovie Medical Corporation Dba Apyx Medical Corporation: 1 (https://510kreport.com/company/bovie-medical-dba-apyx-medical)
- Sound Surgical Technologies, LLC: 1 (https://510kreport.com/company/sound-surgical-technologies)

## Firms that cite its devices most
- Nouvag AG: 1 (https://510kreport.com/company/nouvag)

## Its most-cited devices
- K223262: Renuvion® APR Handpiece (2023), cited by 2
- K244050: AYON Body Contouring System (AYON SYSTEM) (2025), cited by 1
- K230272: Renuvion® APR Handpiece (2023), cited by 1

## Recent decisions
- K261710: AYON™ Power Liposuction Cannulas and AYON™ Power Liposuction Cannula Adaptors (Aug 21, 2026)
- K253396: AYON Body Contouring System™  (AYON SYSTEM) (May 8, 2026)
- K244050: AYON Body Contouring System (AYON SYSTEM) (May 12, 2025)
- K230586: Renuvion® Micro Handpiece (Jun 9, 2023)
- K230272: Renuvion® APR Handpiece (Apr 27, 2023)
- K223262: Renuvion® APR Handpiece (Feb 23, 2023)
- K221830: Apyx One Console (Oct 11, 2022)

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