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 Broadwest Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 4, 1987: PODODIGITAL.
| Date | Record | Source |
|---|---|---|
| Feb 4, 1987 | PODODIGITALK864569 · IKE | 510(k) clearances |
| Feb 4, 1987 | PODOSCOPEK864499 · IKE | 510(k) clearances |
| Jul 2, 1985 | INOX IORCEPS JARK852302 · | 510(k) clearances |
| Jul 1, 1985 | INOX THERMOMETER JARK852301 · FLK | 510(k) clearances |
| Jun 20, 1985 | INOX IV STANDK852300 · FOX | 510(k) clearances |
| May 9, 1985 | INOX DRY HEAT STERILIZERK851307 · KMH | 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
