Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Apyx Medical and its 1 subsidiaries with 11 510(k) clearances. The most recent is a 510(k) clearance dated Aug 21, 2026: AYON™ Power Liposuction Cannulas and AYON™ Power Liposuction Cannula Adaptors.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Apyx Medical and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 21, 2026 | AYON™ Power Liposuction Cannulas and AYON™ Power Liposuction Cannula AdaptorsK261710 · QPB | 510(k) clearances |
| May 8, 2026 | AYON Body Contouring System™ (AYON SYSTEM)K253396 · QPB | 510(k) clearances |
| May 12, 2025 | AYON Body Contouring System (AYON SYSTEM)K244050 · QPB | 510(k) clearances |
| Jun 9, 2023 | Renuvion® Micro HandpieceK230586 · GEI | 510(k) clearances |
| Apr 27, 2023 | Renuvion® APR HandpieceK230272 · GEI | 510(k) clearances |
| Feb 23, 2023 | Renuvion® APR HandpieceK223262 · GEI | 510(k) clearances |
| Oct 11, 2022 | Apyx One ConsoleK221830 · GEI | 510(k) clearances |
| Jul 15, 2022 | Renuvion APR HandpieceK220970 · GEI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built