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 Barriermed Glove Co. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 5, 2006: BARRIERPLUS GOLD POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES.
| Jul 5, 2006 | BARRIERPLUS GOLD POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVESK053406 · KGO | 510(k) clearances |
| Jun 23, 2006 | BARRIERPLUS PLATINUM POWDER-FREE SYNTHETIC POLYCHLOROPRENE SURGICAL GLOVES, MODELS 12544-125490K061038 · KGO | 510(k) clearances |
| Dec 20, 2005 | BARRIERPLUS GOLD ORTHO POWDER-FREE SYNTHETIC POLYISOPRENE ORTHOPEDIC SURGICAL GLOVESK052772 · KGO | 510(k) clearances |
| Nov 30, 2005 | SYNTHALON PC PLUS POWDER-FREE POLYCHLOROPRENE EXAMINATION GLOVES, MODELS 1372-11 TO 1272-55K052892 · LZA | 510(k) clearances |
| May 20, 1999 | BARRIERPLUS SYNTHETIC POWDER-FREE SURGICAL GLOVESK990710 · KGO | 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
