Company · US
Apyx Medical Corporation
FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2026. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (2 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 21, 2026 | K261710 | AYON Power Liposuction Cannulas and AYON Power Liposuction Cannula Adaptors Apyx Medical Corporation | QPB |
| May 8, 2026 | K253396 | AYON Body Contouring System (AYON SYSTEM) Apyx Medical Corporation | QPB |
| May 12, 2025 | K244050 | AYON Body Contouring System (AYON SYSTEM) Apyx Medical Corporation | QPB |
| Jun 9, 2023 | K230586 | Renuvion® Micro Handpiece Apyx Medical Corporation | GEI |
| Apr 27, 2023 | K230272 | Renuvion® APR Handpiece Apyx Medical Corporation | GEI |
| Feb 23, 2023 | K223262 | Renuvion® APR Handpiece Apyx Medical Corporation | GEI |
| Oct 11, 2022 | K221830 | Apyx One Console Apyx Medical Corporation | GEI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||