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 14, 2026, FDA's public records list W.E. Leder Enterprises with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 3, 1983: ARF 850 E.
| Nov 3, 1983 | ARF 850 EK831877 · CBK | 510(k) clearances |
| Sep 29, 1983 | LARYNGESCOPEK831981 · CCW | 510(k) clearances |
| Sep 29, 1983 | CARDIO-SCOPE MINI MONITORK831878 · DPS | 510(k) clearances |
| Mar 9, 1983 | ANESTHESIA APPARATUS PH-35K830159 · BSZ | 510(k) clearances |
| Mar 9, 1983 | ANESTHESIA APPARATUS #FO 20SK830160 · BSZ | 510(k) clearances |
| Mar 9, 1983 | ANESTHESIA APATATUS #D-25K830161 · BSZ | 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
