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 15, 2026, FDA's public records list W.A. Rubbermate Co., Ltd. and its 1 subsidiaries with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 13, 2024: Black Nitrile Powder Free Patient Examination Glove, Non Sterile.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, W.A. Rubbermate Co., Ltd. and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 13, 2024 | Black Nitrile Powder Free Patient Examination Glove, Non SterileK233740 · LZA | 510(k) clearances |
| Jul 13, 2011 | POWDER FREE NITRILE EXAMINATION GLOVESK110418 · LZA | 510(k) clearances |
| Jul 30, 2002 | WA RUBBERMATE LATEX POWDER-FREE EXAM GLOVESK021041 · LYY | 510(k) clearances |
| Aug 29, 1997 | W.A.K971200 · LYY | 510(k) clearances |
| Apr 12, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K891877 · 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
