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 13, 2026, FDA's public records list Laivan Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 31, 1993: TOTAL PROTECTIVE BREATHEABLE SURGICAL GOWNS.
| Date | Record | Source |
|---|---|---|
| Mar 31, 1993 | TOTAL PROTECTIVE BREATHEABLE SURGICAL GOWNSK923815 · FYA | 510(k) clearances |
| Apr 17, 1989 | MODIFIED LABELING FOR POLYDERM WBC(TM)K890940 · NAD | 510(k) clearances |
| Mar 29, 1989 | AQUADERMK885205 · KGX | 510(k) clearances |
| Apr 13, 1988 | POLYDERM A+B(TM)K880153 · NAD | 510(k) clearances |
| Mar 17, 1988 | POLYDERM PEC(TM), POROUS ELASTIC COVERK880964 · KGX | 510(k) clearances |
| Mar 11, 1988 | POLYDERM WBC (TM), WATERPROOF BREATHABLE COVERK880206 · NAD | 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
