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 Ampri Rubberware Industries Sdn Bhd with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 1, 1999: ABSOGEL CHEMOTHERAPHY GLOVES.
| Nov 1, 1999 | ABSOGEL CHEMOTHERAPHY GLOVESK990677 · LZC | 510(k) clearances |
| May 4, 1999 | POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELING CLAIM (CONTAINS 50 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTAK990812 · LYY | 510(k) clearances |
| Jan 29, 1996 | AMPRIK954002 · KGO | 510(k) clearances |
| Sep 5, 1995 | AMPRIK952833 · LYY | 510(k) clearances |
| Jul 31, 1995 | ABSOGEL STERILE POWDER-FREE SURGICAL GLOVESK945948 · KGO | 510(k) clearances |
| Jul 20, 1995 | ABSOGEL NON-STERILE EXAMINATION GLOVES (POWDER-FREE)K946056 · LYY | 510(k) clearances |
| Sep 6, 1989 | CORRECT TOUCH SURGEONS GLOVESK892176 · KGO | 510(k) clearances |
| Aug 25, 1989 | CORRECT TOUCH EXAMINATION GLOVES (LATEX)K892175 · 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
