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 15, 2026, FDA's public records list Oehm und Rehbein with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 24, 2018: AMADEO M-DR mini, AMADEO M-AX mini.
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.
| Sep 24, 2018 | AMADEO M-DR mini, AMADEO M-AX miniK182317 · IZL | 510(k) clearances |
| Aug 29, 2014 | DICOMPACS DX-R WITH FLAT PANELK141440 · MQB | 510(k) clearances |
| Nov 5, 2013 | DICOMPACS DX-R WITH FLAT PANELK131211 · MQB | 510(k) clearances |
| Dec 11, 2009 | DICOMPACS, MODEL 5.2, DICOMPACS DX-R, MODEL 1.4K091364 · LLZ | 510(k) clearances |
| Apr 25, 2007 | DICOMPACS, MODEL 5K070618 · LLZ | 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
