Medical device makerLabelled 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 Reprise Biomedical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 19, 2024: Miro3D Fibers Wound Matrix.
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.
| Apr 19, 2024 | Miro3D Fibers Wound MatrixK240753 · KGN | 510(k) clearances |
| Mar 1, 2024 | MiroDry Wound MatrixK240277 · KGN | 510(k) clearances |
| Dec 13, 2023 | MiroTract Wound MatrixK231614 · KGN | 510(k) clearances |
| Nov 21, 2022 | Miro3D Wound MatrixK223257 · KGN | 510(k) clearances |
| Aug 18, 2022 | Miro3D Wound MatrixK221520 · KGN | 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
