Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Leach and Dillon Co., Inc. with 31 510(k) clearances. The most recent is a 510(k) clearance dated Mar 15, 1991: WIRON 99 DENTAL CASTING ALLOY.
| Mar 15, 1991 | WIRON 99 DENTAL CASTING ALLOYK903538 · EJH | 510(k) clearances |
| Oct 24, 1990 | 250 SL DENTAL CASTING ALLOYK903537 · EJT | 510(k) clearances |
| Oct 5, 1990 | HIGH FUSING WHITE CERAMIC SOLDERK895058 · EJT | 510(k) clearances |
| Oct 5, 1990 | HIGH FUSING YELLOW CERAMIC SOLDERK895059 · EJT | 510(k) clearances |
| Sep 14, 1990 | SELECT 20, DENTAL ALLOYK903484 · EJT | 510(k) clearances |
| Jun 28, 1990 | 200 SILHOUETTE LINE (SL) CERAMIC SOLDERK902373 · EJT | 510(k) clearances |
| Jun 28, 1990 | SILVER-FREE CERAMIC SOLDER (SFCS)K902372 · EJT | 510(k) clearances |
| Apr 10, 1990 | SILHOUETTE PORCELAINK895888 · EIH | 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
