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 L.O.N. Research with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 14, 1989: DISPOSABLE TRANSDUCER MANIFOLD.
| Jul 14, 1989 | DISPOSABLE TRANSDUCER MANIFOLDK890676 · DTL | 510(k) clearances |
| Mar 22, 1988 | ANGIOPLASTY BALLOON INFLATION DEVICEK880158 · LIT | 510(k) clearances |
| Dec 3, 1985 | L.O.N. PRES MON LINES, CPC LINES, ADMINISTRATIONK853099 · DTL | 510(k) clearances |
| Dec 2, 1981 | L.O.N. REUSABLE MANIFOLDS & STOPCOCKSK812407 · DTL | 510(k) clearances |
| Dec 2, 1981 | L.O.N. DISPOSABLE CORONARY MANIFOLDK812408 · DTL | 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
