Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 4 companies' records, each linked to the record.
As of Nov 14, 2026, FDA's public records list Semperit and its 4 subsidiaries with 11 510(k) clearances. The most recent is a 510(k) clearance dated Jan 27, 2023: Non-Sterile, Single use, Powder-free examination glove, Blue, tested for use with Chemot….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Semperit 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
