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 Devoro Medical, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 29, 2024: SmartClaw™ Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw™ Thrombectomy Catheter, 3….
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.
| May 29, 2024 | SmartClaw™ Thrombectomy Catheter, 20 mm (FD0660-01), SmartClaw™ Thrombectomy Catheter, 32 mm (FD0660-02)K241207 · QEW | 510(k) clearances |
| Nov 10, 2022 | WOLF Thrombectomy™ SmartClaw CatheterK221391 · QEW | 510(k) clearances |
| Oct 19, 2021 | WOLF Thrombectomy System, 14FK210911 · QEW | 510(k) clearances |
| Aug 27, 2021 | WOLF Thrombectomy System, 6FK210530 · QEW | 510(k) clearances |
| Apr 27, 2020 | WOLF Thrombectomy V SystemK200101 · QEW | 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
