Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GetingeLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Getinge Disinfection AB with 8 device recalls and 1 510(k) clearance. The most recent is a device recall dated Jul 30, 2013: Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The ….
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.
| Jul 30, 2013 | Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in healthcare facilities Class II · Getinge Disinfection AB initiated a voluntary field safety correction for the Getinge 46-Series electrically-heated Wash | Device recalls |
| Oct 19, 1995 | DECOMAT 4656K950566 · LDS | 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
