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 Denley Instruments, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1992: WELLWASH 4 MARK II.
| Date | Record | Source |
|---|---|---|
| Nov 5, 1992 | WELLWASH 4 MARK IIK922803 · JQW | 510(k) clearances |
| Aug 12, 1992 | DENLEY WELLPREP 2 SAMPLE PROCESSORK922327 · JQW | 510(k) clearances |
| Aug 11, 1992 | WELLPREP 2000 SAMPLE PROCESSORK922183 · JQW | 510(k) clearances |
| Jan 22, 1992 | STACKING MICROPLATE WASHERK915284 · JQW | 510(k) clearances |
| Oct 4, 1991 | WELLPREP 1K913567 · JQW | 510(k) clearances |
| May 17, 1990 | MICROPLATE REAGENT DISPENSERK900599 · JQW | 510(k) clearances |
| Aug 21, 1989 | DENLEY ANTHOS 2001 READERK894270 · JJQ | 510(k) clearances |
| Aug 21, 1989 | DENLEY WELLDILL 3K894272 · JQW | 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
