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 3MLabelled 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 3M Deutschland with 12 510(k) clearances. The most recent is a 510(k) clearance dated Feb 1, 2022: Permadyne.
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.
| Feb 1, 2022 | PermadyneK220257 · ELW | 510(k) clearances |
| Nov 5, 2019 | Suglue 3K192992 · EMA | 510(k) clearances |
| Oct 31, 2019 | ADH19K192961 · KLE | 510(k) clearances |
| Oct 31, 2017 | Rapid HB, Rapid LB, Rapid MBK173318 · ELW | 510(k) clearances |
| Sep 1, 2016 | XP202K161922 · EIH | 510(k) clearances |
| Apr 13, 2016 | Ketac Universal AplicapK153174 · EMA | 510(k) clearances |
| Mar 11, 2016 | Clean & MoreK151748 · PIP | 510(k) clearances |
| Sep 14, 2015 | SuPro 100K151144 · EBG | 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
