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 N.M. Beale Co. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 4, 2011: EZ-MISTER.
| Date | Record | Source |
|---|---|---|
| Mar 4, 2011 | EZ-MISTERK093584 · CCT | 510(k) clearances |
| Feb 16, 2010 | SCOPE INTRODUCER MODEL 7400K093329 · ODC | 510(k) clearances |
| Nov 20, 2007 | PEF TUBEK071579 · KNT | 510(k) clearances |
| May 12, 2000 | BALLOON FOR ULTRASONIC ENDOSCOPESK992178 · ITX | 510(k) clearances |
| Sep 24, 1990 | N. M. BEALE COMPANY VU-THRU WATER BOTTLEK903834 · OCX | 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
