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 15, 2026, FDA's public records list Ventris Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 2, 2026: Collagen Wound Powder.
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.
| Jul 2, 2026 | Collagen Wound PowderK260596 · KGN | 510(k) clearances |
| Mar 21, 2025 | Porous Biologic ScaffoldK250556 · MQV | 510(k) clearances |
| Dec 18, 2024 | Porous Biologic ScaffoldK240765 · MQV | 510(k) clearances |
| Mar 7, 2024 | Synthetic Bone PuttyK240458 · MQV | 510(k) clearances |
| Sep 2, 2022 | Synthetic Bone PuttyK221644 · MQV | 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
