Apyx Medical Corporation

FDA Regulatory Profile

Apyx Medical Corporation appears in FDA public data with 0 recalls, 7 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 21, 2026.

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261710AYON™ Power Liposuction Cannulas and AYON™ Power Liposuction Cannula AdaptorsAugust 21, 2026
K253396AYON Body Contouring System™ (AYON SYSTEM)May 8, 2026
K244050AYON Body Contouring System (AYON SYSTEM)May 12, 2025
K230586Renuvion® Micro HandpieceJune 9, 2023
K230272Renuvion® APR HandpieceApril 27, 2023
K223262Renuvion® APR HandpieceFebruary 23, 2023
K221830Apyx One ConsoleOctober 11, 2022