Medical device makerLabelled 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 13, 2026, FDA's public records list Ilooda with 16 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2024: Secret MAX Multi-platform RF System.
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.
| Date | Record | Source |
|---|---|---|
| Nov 21, 2024 | Secret MAX Multi-platform RF SystemK241157 · GEI | 510(k) clearances |
| Aug 13, 2024 | SUPER VELOCEK241699 · GEX | 510(k) clearances |
| Dec 14, 2023 | Secret ProK233374 · GEI | 510(k) clearances |
| Sep 15, 2023 | PENTO Nd:YAG and Alexandrite laser systemK231791 · GEX | 510(k) clearances |
| Sep 27, 2022 | MTX-C1K212561 · GEI | 510(k) clearances |
| Sep 23, 2022 | reepot Nd; YAG laser systemK222555 · GEX | 510(k) clearances |
| Jun 24, 2022 | Secret DuoK213250 · GEX | 510(k) clearances |
| Jun 9, 2022 | ACUTRONK211000 · 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
