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 8 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Smith & Nephew and its 31 subsidiaries with 1,255 510(k) clearances, 325 device recalls and 44 drug applications. The most recent is a 510(k) clearance dated Oct 30, 2026: RENASYS-G 15Fr Channel Drain Gauze Dressing Kit (66802257); RENASYS 15Fr Channel Drain A….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Smith & Nephew and its 31 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
