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 Ackermann Instrumente GmbH with 3 510(k) clearances. The most recent is a 510(k) clearance dated Sep 16, 2015: Ackermann Intervertebral Body Fusion Device.
| Date | Record | Source |
|---|---|---|
| Sep 16, 2015 | Ackermann Intervertebral Body Fusion DeviceK143450 · ODP | 510(k) clearances |
| Nov 8, 2011 | ACKERMANN EUROPCLIPK111930 · FZP | 510(k) clearances |
| Apr 21, 1998 | ACKERMANN SURGICAL INSTRUMENTSK974382 · GCJ | 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
