Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Medigloves, Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 13, 2005: MEDIGLOVES STERILE POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES.
| Apr 13, 2005 | MEDIGLOVES STERILE POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVESK050181 · KGO | 510(k) clearances |
| Feb 3, 1994 | MEDIGLOVES, MEDPAC, BOSTON, FISHERBRAND, GLOVESK930794 · KGO | 510(k) clearances |
| Feb 3, 1994 | MEDIGLOVES, FISHERBRAND, MEDIPRODUCTS GLOVESK930795 · LYY | 510(k) clearances |
| Sep 6, 1991 | HYPOALLERGENIC EXAMINATION LATEX GLOVESK912503 · LYY | 510(k) clearances |
| Sep 6, 1991 | HYPOALLERGENIC SURGICAL LATEX GLOVESK912157 · KGO | 510(k) clearances |
| Sep 13, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K891326 · LYY | 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
