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 16 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Medline Industries and its 4 subsidiaries with 1,512 device recalls, 276 510(k) clearances, 88 drug recalls, 2 warning letters and 1 drug application. The most recent is a 510(k) clearance dated Jul 29, 2026: NAMIC Dilator and Sheath.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Medline Industries and its 4 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
