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 its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Erchonia with 26 510(k) clearances. The most recent is a 510(k) clearance dated Feb 19, 2026: Erchonia DPN Laser (Model# EVRL).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 19, 2026 | Erchonia DPN Laser (Model# EVRL)K251903 · NHN | 510(k) clearances |
| Dec 15, 2025 | Erchonia CLX (Model # CFL)K252574 · OLI | 510(k) clearances |
| Sep 12, 2025 | Erchonia EVRLK251843 · OLP | 510(k) clearances |
| Jan 10, 2025 | Erchonia Zerona® VZ8K243811 · OLI | 510(k) clearances |
| Aug 11, 2023 | Erchonia FX-405K231409 · NHN | 510(k) clearances |
| Jul 21, 2023 | Erchonia Violet ZERONA® Z6 OTCK231474 · OLI | 510(k) clearances |
| Sep 1, 2022 | Erchonia GVLK221987 · NHN | 510(k) clearances |
| Mar 24, 2022 | Erchonia Zerona Z-BedK220519 · OLI | 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
