Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in MalaysiaLabelled 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 Latexx Partners Bhd. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 2001: NON-CHLORINATED, POLYMER COATED POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES.
| Aug 1, 2001 | NON-CHLORINATED, POLYMER COATED POWDER-FREE NITRILE PATIENT EXAMINATION GLOVESK011792 · LZA | 510(k) clearances |
| Aug 1, 2001 | POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLORK011791 · LZA | 510(k) clearances |
| Nov 5, 1999 | QTEXX, NON-CHLORINATED, POWDER FREE NITRILE EXAMINATION GLOVES, POLYMER-COATEDK992924 · LZA | 510(k) clearances |
| Sep 24, 1999 | QTEXX PRE-POWDERED NITRILE EXAMINATION GLOVESK992671 · LZA | 510(k) clearances |
| May 28, 1999 | QTEXX POWDER FREE LATEX EXAMINATION GLOVES, POLYMER COATEDK991462 · LYY | 510(k) clearances |
| Jun 11, 1998 | QTEXX POWDERFREE LATEX EXAMINATION GLOVESK981767 · LYY | 510(k) clearances |
| Jun 1, 1998 | PROFLEX POWDER FREE NITRILE EXAMINATION GLOVESK981159 · LZA | 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