Medical device makerLabelled 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 Sauter AG with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 17, 2015: BELIMED STEAM STERILIZER MST-H.
| Date | Record | Source |
|---|---|---|
| Jun 17, 2015 | BELIMED STEAM STERILIZER MST-HK141879 · FLE | 510(k) clearances |
| Mar 15, 2011 | BELIMED STEAM STERILIZER MST-VK103841 · FLE | 510(k) clearances |
| Mar 8, 2006 | BELIMED STEAM STERILIZER TOP 5000, MODEL 5-5-9K060337 · FLE | 510(k) clearances |
| Feb 2, 2004 | BELIMED STEAM STERILIZER TOP 5000, SERIES 4 - 8K033538 · FLE | 510(k) clearances |
| Jun 26, 2002 | BELIMED STEAM STERILIZER, MODEL TOP 5000K021223 · FLE | 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
