Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Damon Corp. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 23, 1987: DAMON D.E.T.E.C.T IMAGE ENHANCER.
| Date | Record | Source |
|---|---|---|
| Dec 23, 1987 | DAMON D.E.T.E.C.T IMAGE ENHANCERK874865 · LLZ | 510(k) clearances |
| Jul 18, 1983 | ADRENOCORTICOTROPIN RADIO-IMMUNOASSAYK831826 · CKG | 510(k) clearances |
| Apr 1, 1982 | LIQUISOL PROGESTERONE RADIOIMMUNOK820686 · JLS | 510(k) clearances |
| Dec 10, 1980 | LIQUISOL TESTOSTERONE RADIOIMM. TEST KITK802661 · CDZ | 510(k) clearances |
| Apr 4, 1979 | LIQUISOL CORTISOL RIA TEST KITK790250 · | 510(k) clearances |
| Feb 26, 1979 | IEC CENTRA-7 CENTRIFUGE MODEL 2362K782124 · JQC | 510(k) clearances |
| Jul 27, 1978 | RIA TEST KIT SYS. DAMON KIQUISOL FREEK781012 · CEC | 510(k) clearances |
| Feb 23, 1978 | LIQUISOL DIGOXIN RIA TEST KITK780207 · DON | 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
