Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwitzerlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list NDD Medizintechnik AG with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 19, 2023: EasyOne Sky Spirometer.
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.
| Oct 19, 2023 | EasyOne Sky SpirometerK230178 · BZG | 510(k) clearances |
| Nov 22, 2022 | EasyOne FilterK221250 · CAH | 510(k) clearances |
| Feb 22, 2017 | EasyOne Pro Respiratory Analysis SystemK161534 · BTY | 510(k) clearances |
| Jan 5, 2017 | EasyOne Air SpirometerK161536 · BZG | 510(k) clearances |
| Sep 27, 2012 | EASYONE PRO RESPIRATORY TESTING DEVICEK120635 · BTY | 510(k) clearances |
| Jan 27, 2010 | EASYONE PRO RESPIRATORY ANALYSIS SYSTEMK091428 · BTY | 510(k) clearances |
| Jun 2, 2009 | EASY ON-PC SPIROMETERK090034 · BZG | 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
