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 Aevumed, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 2, 2026: Aevumed SUPERCYNCH™ Button 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 |
|---|---|---|
| Sep 2, 2026 | Aevumed SUPERCYNCH™ Button SystemK253065 · MBI | 510(k) clearances |
| Mar 4, 2026 | Aevumed FENIX Suture AnchorK254306 · MBI | 510(k) clearances |
| Jan 28, 2026 | Aevumed PROTEKT Suture AnchorK260004 · MBI | 510(k) clearances |
| Oct 21, 2025 | Aevumed FASE Suture AnchorK253040 · MBI | 510(k) clearances |
| Aug 6, 2025 | Aevumed PHANTOM Suture AnchorsK242895 · MBI | 510(k) clearances |
| Mar 17, 2023 | Aevumed RAPID Suture AnchorsK223878 · MBI | 510(k) clearances |
| Nov 28, 2022 | Aevumed PHANTOM™-LP Suture AnchorsK222363 · MBI | 510(k) clearances |
| May 31, 2018 | AEVUMED PHANTOM Suture AnchorsK180464 · MBI | 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
