Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 14, 2026, FDA's public records list General Electric and its 17 subsidiaries with 688 510(k) clearances and 40 device recalls. The most recent is a 510(k) clearance dated Jul 24, 2026: Monitor B105M; Monitor B125M; Monitor B155M; Monitor B105P; Monitor B125P.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, General Electric and its 17 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
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
