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 Transworld X-Ray Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 23, 1989: SENSIMAT.
| Jun 23, 1989 | SENSIMATK892657 · IZO | 510(k) clearances |
| Mar 28, 1989 | STAR 36K890066 · IZO | 510(k) clearances |
| Sep 10, 1987 | MODEL C2-5000 OVERHEAD TUBE SUPPORTK873283 · IYB | 510(k) clearances |
| Aug 27, 1987 | MAM-CP X-RAY APPARATUSK872980 · IZH | 510(k) clearances |
| Jul 15, 1987 | TRANSWORLD 360V, MODEL A1-4040K872357 · IZO | 510(k) clearances |
| Aug 10, 1984 | DCX-100 CHEST UNIT-GL-5000MK841923 · KPR | 510(k) clearances |
| Jul 9, 1982 | MODIFIED X-RAY TABLEK827582 · | 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
