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., part of Ion Beam ApplicationsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list IBA Dosimetry GmbH with 6 device recalls and 3 510(k) clearances. The most recent is a device recall dated Apr 1, 2025: myQA iON; Article Number: MQ10-000;.
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.
| Apr 1, 2025 | myQA iON; Article Number: MQ10-000;Class II · Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a sp | Device recalls |
| Jul 17, 2020 | myQA iONK201798 · LHN | 510(k) clearances |
| Jan 23, 2020 | Blue Phantom PTK191821 · LHN | 510(k) clearances |
| Sep 18, 2009 | OMNIPRO INCLINEK092018 · IYE | 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
