Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Aktormed GmbH with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 20, 2026: ENDOSCOPE HOLDER (182214).
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 |
|---|---|---|
| Jul 20, 2026 | ENDOSCOPE HOLDER (182214)K261573 · QZB | 510(k) clearances |
| Aug 8, 2024 | SOLOASSIST IID / DEXTER ENDOSCOPE ARM (212499); ARTip solo (202426) + ARTip solo voice (202445); SOLOASSIST II (141364) + VOICE CONTROL (171894K233312 · QZB | 510(k) clearances |
| Apr 25, 2024 | ENDOFIX EXOK232405 · OCV | 510(k) clearances |
| Dec 22, 2020 | SoloAsisst II, Voice ControlK200473 · NAY | 510(k) clearances |
| Sep 21, 2018 | SOLOASSIST IIK171947 · NAY | 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
