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 13, 2026, FDA's public records list Deringer-Ney, Inc. with 46 510(k) clearances. The most recent is a 510(k) clearance dated Oct 14, 1993: GDC 3509.
| Date | Record | Source |
|---|---|---|
| Oct 14, 1993 | GDC 3509K933178 · EJT | 510(k) clearances |
| Mar 31, 1993 | DENTAL CASTING ALLOY, MODIFICATION - PF-3K930482 · EJT | 510(k) clearances |
| Mar 31, 1993 | DENTAL CASTING ALLOY MODIFICATION-PF-4K930481 · EJT | 510(k) clearances |
| Dec 21, 1992 | GDC 3445K925273 · EJS | 510(k) clearances |
| May 5, 1992 | GDC 3367K920922 · EJS | 510(k) clearances |
| Apr 2, 1992 | DENTAL SOLDER ALLOYK920060 · EJT | 510(k) clearances |
| Mar 19, 1992 | GDC-3338, DENTAL SOLDER ALLOYK920887 · EJS | 510(k) clearances |
| Mar 15, 1991 | GDC-3200 DENTAL SOLDERK910065 · EJT | 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
