Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IndonesiaLabelled 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 PT WRP Buana Multicorpora with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 19, 2003: GLOVETEX POWDER FREE NITRILE EXAMINATION GLOVES, BLUE, NON-STERILE.
| Aug 19, 2003 | GLOVETEX POWDER FREE NITRILE EXAMINATION GLOVES, BLUE, NON-STERILEK032010 · LZA | 510(k) clearances |
| Aug 19, 2003 | GLOVETEX POWDER FREE WHITE NITRILE EXAMINATION GLOVES, NON-STERILEK032011 · LZA | 510(k) clearances |
| Jul 28, 2003 | GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, BLUE, NON-STERILE CONTAINS 50 MCGIN OR LESS OF TOTAL WATER EXTRACTABLE PRK032007 · LYY | 510(k) clearances |
| Mar 26, 2003 | GLOVETEX LATEX EXAMINATION GLOVES, POWDERED, BLUE, NON STERILEK030273 · LYY | 510(k) clearances |
| Sep 16, 2002 | GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, NON STERILE (PROTEIN CONTENT LABELING CLAIM 50UG/G OR LESS)K022343 · LYY | 510(k) clearances |
| May 23, 2000 | GLOVETEX, LATEX EXAMINATION GLOVES, POWDERED NON-STERILE.(PROTEIN CONTENT LABELING)K994426 · 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
